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Shutt Series 210, Aggressor

by Conmed Corporation 2 variants

Ref S210AFL, 9899, S210MSC, S210AFU, S210GSP, S210SRF

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10845854031490 Basic UDI-DI Date29 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10845854031490 UDI-DI Date14 Oct 2021ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Shutt Series 210, Aggressor
Shutt
Generic Name
Surgical soft-tissue manipulation forceps, scissors-like, reusable
Instrument tray, reusable
General-purpose surgical scissors, reusable
Device Name
Orthopedic, Non-active, Reusable Surgical Instrument, Cutting
Orthopedic, Non-active, Instrument Tray
Model / Ref / Catalog
S210AFL, 9899, S210MSC, S210AFU, S210GSP, S210SRF
Primary DI / UDI-DI
10845854031490, 10845854026328, 10845854031520, 10845854031513, 10845854028742, 10845854031551
Basic UDI-DI
B-10845854031490, 084585408521D5, B-10845854031520, B-10845854031513, B-10845854028742, B-10845854031551
Direct Marketing DI
20845854026325
FDA Product Code
GEN, FSM, LXH
EMDN Code
L090903, S010401, L03130401
GMDN Term
Surgical soft-tissue manipulation forceps, scissors-like, reusable
Instrument tray, reusable
General-purpose surgical scissors, reusable
Device Class
Class I
Regulation Number
878.4800, 888.4540
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Manufacturer details

EUDAMED SRN
US-MF-000012663
Authorised representative
MDSS GmbH DE-AR-000005430

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Reusable YesEUDAMEDNoEUDAMED
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (19)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No