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Aesculap AG

Active in EUDAMED

Germanyfrom SRN EUDAMED FDA SRN DE-MF-000005504 FEI 3002806315

Aesculap AG is a medical device manufacturer based in Germany, with 23,926 devices listed as of 13 Nov 2026.

Devices
23,926
Registrations
EUDAMEDFDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • EUDAMED 3,000
  • FDA GUDID 3,000

Among the 3,000 best-ranked of 23,926 devices.

Device classes
  • FDA Class I 1,613
  • FDA Class II 1,386
  • EU Class I 1

Among the 3,000 best-ranked of 23,926 devices.

Top EMDN categories

Among the 3,000 best-ranked of 23,926 devices.

Identifiers
  • EUDAMED SRN DE-MF-000005504
  • FDA FEI 3002806315
  • DUNS 315018218

At a glance

Counted by deviCERTS from registry records

EU certificates

5 of 6 in force. 1 certificate has expired.

See certificates

Market reach

European Union
EUDAMED actor, 6 certificates
United States
FDA establishment

What Aesculap AG makes

Aesculap AG manufactures reusable surgical instruments, including bone-screw internal spinal fixation connectors, suturing needle holders, general-purpose scissors, and bone curettes. Their portfolio also includes spinal bone screws (non-bioabsorbable), endodontic files/rasps, and systems for plume evacuation during surgery. Specialized devices like the S4® spinal fixation system and the PLASMAFIT plume evacuation tube are part of their product range.

These devices are classified under EU Medical Device Regulations as Class I, Class IIa, and Class IIb. They are registered in the EU’s eudamed database, a centralised repository for medical device information. The company is headquartered in Germany.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue23,926

Newest first, rows 1-50 of 23,926

Search and filter all 23,926 devices
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  • Prevision Ref NT1264R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Targon Pf Ref KH419T

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NT1386R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NG803R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Targon Pf Ref KH355P

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NG824R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NG813R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NG821R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NT1254

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Insitucat® Ref 5521106

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa

  • Prevision Ref NG867R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Bicontact Revision Ref NF503R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NG814R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Targon Fn Ref KT230R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Targon Pf Ref KH368R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NG834R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Targon Pf Ref KH399T

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NT1394R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NG836R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NG827R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Targon Pf Ref KH374R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NT1352R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Targon Pf Ref KH361P

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NT1262R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NT1313R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NT1365R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NT1317R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Targon Pf Ref KH360P

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NG764R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Targon Fn Ref KT235P

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NG817R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NT1312

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref ND552

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NT1362R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NG595R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NG845R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NG812R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NT1314

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Targon Pf Ref KH391P

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NT1375R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NT1255

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Aesculap Ref NT1345R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NT1376R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Bicontact Ref NG114R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NT1263R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NT1321R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NT1299R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NT1310

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NT1323R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

  • Prevision Ref NT1303R

    Active Regimes: CE MDR Registry: EUDAMED Class:I

Rows 1-50 of 23,926

Showing 1-50 of 23,926

Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
DE-MF-000005504
FDA FEI number
3002806315
DUNS number
315018218
EUDAMED status
Active
EUDAMED registered name
Aesculap AG
Registered address
Am Aesculap-Platz, 78532, Tuttlingen, Germany
Phone
+1(800)282-9000
PRRC contact
Jacqueline Liebers(public in EUDAMED)

EUDAMED certificates6

6 certificates5 valid, 1 expiredMDR 6next expiry 9 Jul 2030

EUDAMED certificates (6)

TÜV SÜD Product Service GmbH 0123 4 certificates

  • G10 010066 0438 Active Reissued

    Quality management system EU MDR

    Issued
    16 May 2025
    Expires
    9 Jul 2030
    Valid from
    10 Jul 2025
  • G11 010066 0437 Active Reissued

    Quality management system EU MDR

    Issued
    5 May 2025
    Expires
    9 Jul 2030
    Valid from
    10 Jul 2025
  • G15 010066 0466 Active Reissued

    Quality management system EU MDR

    Issued
    30 Apr 2026
    Expires
    9 Jul 2030
    Valid from
    1 Jul 2026
  • G12 010066 0441 Expired

    Quality management system EU MDR

    Issued
    20 Aug 2024
    Expires
    30 Jun 2026
    Reason
    Add device or group

DNV MEDCERT GmbH 0482 2 certificates

  • 20201GB450260922 Active Reissued

    Technical documentation EU MDR

    Issued
    22 Sep 2026
    Expires
    7 Oct 2031
    Valid from
    8 Oct 2026
  • 20003GB450260622 Active Reissued

    Technical documentation EU MDR

    Issued
    22 Jun 2026
    Expires
    22 Jun 2031
    Valid from
    23 Jul 2026

FDA establishments2

Registered with the FDA under this company group, matched by name.

  • Aesculap SAS CHAUMONT Grand Est · FR FEI 3001354499
  • Aesculap, Inc. CENTER VALLEY, PA · US FEI 2916714

Frequently asked questions

How many devices does Aesculap AG have in the registry?

The registry currently lists 23926 devices for Aesculap AG. Devices recorded under merged duplicate company entries are counted once.

Which registries list Aesculap AG's devices?

Among its 50 most recently registered devices, Aesculap AG has devices listed in EUDAMED (50 devices).

What risk classes do Aesculap AG's devices fall under?

Among its 50 most recently registered devices, the classes recorded for Aesculap AG's devices are Class I and Class IIa. Each device page shows its own class and authorisation.

What EUDAMED certificates are recorded for Aesculap AG?

EUDAMED lists 6 certificates for Aesculap AG (technical documentation; quality management system) under MDR. The most recent was issued on 22 Sep 2026.

What are the newest devices from Aesculap AG in the registry?

The most recently registered devices listed for Aesculap AG include PREVISION, TARGON PF, Insitucat® and BICONTACT REVISION.

Which FDA establishments are linked to Aesculap AG?

2 FDA establishments are linked to Aesculap AG in the registry; they are listed on the company page.

Generated automatically from registry data and not verified by a human reviewer.