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Aea SRL

Active in EUDAMED

Italyfrom SRN EUDAMED FDA SRN IT-MF-000027519 FEI 3006571738

Aea SRL is a medical device manufacturer based in Italy, with 41 devices listed in EUDAMED, FDA GUDID and FDA 510(k) (FDA Class II; EU Class IIa and I) as of 14 Nov 2026.

Devices
41
Registrations
EUDAMEDFDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 14 Nov 2026

Registries
  • EUDAMED 24
  • FDA GUDID 20
  • FDA 510(k) 3

A device listed in two registries counts in both.

Device classes
  • FDA Class II 18
  • EU Class IIa 14
  • EU Class I 9
Top EMDN categories
Identifiers
  • EUDAMED SRN IT-MF-000027519
  • FDA FEI 3006571738
  • DUNS 429415227

At a glance

Counted by deviCERTS from registry records

EU certificates

1 of 1 in force.

See certificates

Market reach

European Union
EUDAMED actor, 1 certificate
United States
FDA FEI

What Aea SRL makes

AEA SRL manufactures hazardous fluid syringes, general-purpose fluid transfer sets, and pharmaceutical fluid-dispensing systems. Their product range includes dosing devices, filling lines, and specialized syringe units such as the APOTECA system and TE Syringe hive models.

The company is based in Italy, and its portfolio consists of devices classified as Class I, Class II, and Class IIa. These products are listed in the EUDAMED database and are registered with the FDA through 510(k) clearance and UDI requirements.

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

Catalogue41

Newest first, rows 1-41 of 41

Search and filter all 41 devices
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  • Dosing device 50ml Ref ASN-50-P

    Expiring Regimes: CE MDR Registry: EUDAMED Class:IIa

  • B Recon Line with needle Ref BDL-04

    Expiring Regimes: CE MDR Registry: EUDAMED Class:I

  • B Filling Line for bag Ref BDL-06

    Expiring Regimes: CE MDR Registry: EUDAMED Class:I

  • TE Syringe hive 5ml Ref ASH-05-WGR-P

    Expiring Regimes: CE MDR Registry: EUDAMED Class:IIa

  • S dispensing line Ref SDL-01-FIL

    Expiring Regimes: CE MDR Registry: EUDAMED Class:I

  • B Double Filling Line with vial needle Ref BDL-05

    Expiring Regimes: CE MDR Registry: EUDAMED Class:I

  • Dosing device 20ml Ref ASN-20-P

    Expiring Regimes: CE MDR Registry: EUDAMED Class:IIa

  • TE Syringe hive 5ml Ref ASH-10-WGR-P

    Expiring Regimes: CE MDR Registry: EUDAMED Class:IIa

  • Dosing device 5ml Ref ASN-05-P

    Expiring Regimes: CE MDR Registry: EUDAMED Class:IIa

  • B Filling Line Ref BDL-03

    Expiring Regimes: CE MDR Registry: EUDAMED Class:I

  • Dosing device 3ml Ref ASN-03-P

    Expiring Regimes: CE MDR Registry: EUDAMED Class:IIa

  • TE Syringe hive 10ml Ref ASH-10-WGR-B

    Expiring Regimes: CE MDR Registry: EUDAMED Class:IIa

  • APOTECAsyringe

    Listed Registry: GUDID Class:II

  • Apoteca Asn-20-B-Nce

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Apoteca Asn-50-B-Nce

    Active Regimes: 510(k) Registry: GUDID Class:II

  • APOTECA S Dispensing Line

    Expiring Regimes: CE MDR Registry: EUDAMEDGUDID Class:II

  • APOTECA APOTECAchemo

    Listed Registry: GUDID Class:II

  • APOTECA APOTECAunit

    Listed Registry: GUDID Class:II

  • Apoteca ADY1200CF

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Apoteca Asn-05-K-Nce

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Apoteca Asn-05-B-Nce

    Active Regimes: 510(k) Registry: GUDID Class:II

  • APOTECA APOTECAped

    Listed Registry: GUDID Class:II

  • Apoteca ADY1200C

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Apoteca Asn-20-K-Nce

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Apoteca ADY1100CF

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Apoteca ADY1100C

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Apoteca Asn-50-K-Nce

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Dosing device 20ml Ref ASN-20-B

    Expiring Regimes: CE MDR Registry: EUDAMEDGUDID Class:IIa

  • B Recon Line Ref BDL-01

    Expiring Regimes: CE MDR Registry: EUDAMED Class:I

  • B Dispensing Line Ref K203674

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Apoteca Dug Compounding Dosing Device, Apoteca I.V. Transfer Set Ref K132011

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • S dispensing line Ref K192770

    Active Regimes: CE MDR 510(k) Registry: 510(k) Class:II

  • Dosing device 3ml Ref ASN-03-B

    Expiring Regimes: CE MDR Registry: EUDAMEDGUDID Class:IIa

  • TE Syringe hive 5ml Ref ASH-05-WGR-B

    Expiring Regimes: CE MDR Registry: EUDAMED Class:IIa

  • Easy Transfer (White 1 inch) Ref WN-24

    Expiring Regimes: CE MDR Registry: EUDAMED Class:I

  • Dosing device 1ml Ref ASN-01-B

    Expiring Regimes: CE MDR Registry: EUDAMED Class:IIa

  • Dosing device 5ml Ref ASN-05-B

    Expiring Regimes: CE MDR Registry: EUDAMEDGUDID Class:IIa

  • Dosing Device Ref ASN-50-B

    Expiring Regimes: CE MDR Registry: EUDAMEDGUDID Class:IIa

  • Easy Transfer (Red 0.5 inch) Ref RN-12

    Expiring Regimes: CE MDR Registry: EUDAMED Class:I

  • B Double Filling Line Ref BDL-02

    Expiring Regimes: CE MDR Registry: EUDAMED Class:I

  • Dosing device 10ml Ref ASN-10-B

    Expiring Regimes: CE MDR Registry: EUDAMEDGUDID Class:IIa

Rows 1-41 of 41

Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
IT-MF-000027519
FDA FEI number
3006571738
DUNS number
429415227
EU VAT number
00686250424
EUDAMED status
Active
EUDAMED registered name
AEA srl
EUDAMED abbreviated name
LOCCIONI
Registered address
16, via Fiume, 60030, Angeli di Rosora, Italy
PRRC contact
Michele Mengoni(public in EUDAMED)

EUDAMED certificates1

1 certificate1 valid, 0 expiredMDR 1next expiry 9 Aug 2027

EUDAMED certificates (1)

KIWA CERMET ITALIA S.P.A. 0476 1 certificate

  • MDR 00004-A Expiring Expires in 268 days

    Quality management system EU MDR

    Issued
    12 Oct 2026
    Expires
    9 Aug 2027

Frequently asked questions

How many devices does AEA SRL have in the registry?

The registry currently lists 41 devices for AEA SRL. Devices recorded under merged duplicate company entries are counted once.

Which registries list AEA SRL's devices?

Among its 41 most recently registered devices, AEA SRL has devices listed in EUDAMED (24 devices), FDA 510(k) (3 devices) and FDA GUDID (20 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do AEA SRL's devices fall under?

Among its 41 most recently registered devices, the classes recorded for AEA SRL's devices are Class I, Class IIa and Class II. Each device page shows its own class and authorisation.

What EUDAMED certificates are recorded for AEA SRL?

EUDAMED lists 1 certificate for AEA SRL (quality management system) under MDR. 1 is recorded with the status issued. The most recent was issued on 12 Oct 2026.

What are the newest devices from AEA SRL in the registry?

The most recently registered devices listed for AEA SRL include Dosing device 50ml, B Recon Line with needle, B Filling Line for bag and TE Syringe hive 5ml.

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