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Hawkins

by Argon Medical Devices, Inc. 7 variants

Ref 216057, 243030, 251100

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-20886333003567 Basic UDI-DI Date5 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number20886333003567 UDI-DI Date29 Jun 2022ListedStatusListed 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  • Withdrawn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
Hawkins EUDAMED
Breast Localization Needles GUDID
Hawkins™ Blunt Needle GUDID
Generic Name
Radiological image marker, implantable
Closed-wound drainage kit, micro-drainage
Device Name
Hawkins Blunt Needle
Hawkins III Hardwire BLN
Model / Ref / Catalog
216057, 243030, 251100
Description
Hawkins™ III Hardwire BLN 20ga x 3cm
Hawkins™ Blunt Needle 16ga x 5cm
Hawkins™ I BLN 20ga x 10cm
Primary DI / UDI-DI
20886333003567 EUDAMED
20886333003727 EUDAMED
20886333003789 EUDAMED
00886333003723 GUDID
00886333003563 GUDID
00886333003785 GUDID
Basic UDI-DI
B-20886333003567, B-20886333003727, B-20886333003789
FDA Product Code
GDM, KNW
EMDN Code
A0680, A019012
GMDN Term
Radiological image marker, implantable
Closed-wound drainage kit, micro-drainage
Device Class
Class IIa EUDAMED
Class I GUDID
Class II GUDID
Regulation Number
878.4800, 876.1075
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 3 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
20886333003567
20886333003727
20886333003789
GUDID
00886333003723
00886333003563
00886333003785
Device ClassEUDAMED
Class IIa
GUDID
Class I
Class II
ImplantableEUDAMED
No
GUDID
No
Yes

Manufacturer details

EUDAMED SRN
US-MF-000002324
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from Argon Medical Devices, Inc.

See all devices from Argon Medical Devices, Inc. →

Properties

  • Sterile
  • Single Use
  • Implantable NoEUDAMEDGUDIDYesGUDID
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (15)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No