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Jawz Endomyocardial Biopsy Forcep 190065

by Argon Medical Devices, Inc.

Ref 190065

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

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None found

in data synced 22 Oct 2026

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-20886333206777 Basic UDI-DI 20886333206777UDI-DIDate11 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number20886333206777 UDI-DI Date16 Sep 2016ListedStatusListed 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.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

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  • Withdrawn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
JAWZ Biopsy Forceps EUDAMED
Jawz Endomyocardial Biopsy Forcep GUDID
Generic Name
Endomyocardial biopsy forceps, single-use
Model / Ref / Catalog
190065
Primary DI / UDI-DI
20886333206777 EUDAMED
00886333206773 GUDID
Basic UDI-DI
B-20886333206777
510(k) Number
FDA Product Code
DWZ
EMDN Code
C01901102 Myocardial biopsy kits
GMDN Term
Endomyocardial biopsy forceps, single-use
Device Class
Class III EUDAMED
Class II GUDID
Regulation Number
870.4075
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
20886333206777
GUDID
00886333206773
Device ClassEUDAMED
Class III
GUDID
Class II

Related devices

Cleared under the same submission (K951447)

Show all (12)

Other devices from Argon Medical Devices, Inc.

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Properties

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

Other properties (16)

  • Implantable: No
  • 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