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Verbandpäckchen M, 8cm x 10cm, DIN 13151

by Hans Hepp GmbH & Co. KG

Ref 60004, 92210, 88155

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

CE MDR 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
United StatesGUDID listing GUDID Number04007418600040 UDI-DI Date25 Jul 2023ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED NumberB-04007418600040 Basic UDI-DI Date27 Jun 2022RegisteredStatusActive
European UnionCE/MDD EUDAMED NumberB-04007418600040 Basic UDI-DI Date27 Jun 2022RegisteredStatusActive

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  • Withdrawn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/MDR, CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Verbandpäckchen M, 8cm x 10cm, DIN 13151 EUDAMED
Verbandpäckchen M, 8 cm x 10 cm, DIN 13151 EUDAMED
First Aid Dressing M Compress 8cm x 10cm GUDID
Generic Name
First aid absorbent pad/bandage
Device Name
Verbandpäckchen
Model / Reference
60004, 92210, 88155
Primary DI / UDI-DI
04007418600040, 04007418922104, 04007418881555
Basic UDI-DI
B-04007418600040, B-04007418922104, B-04007418881555, 4007418VerbandpaeckchenJ3
FDA Product Code
MHW
EMDN Code
M040204 Non-adherent absorbent dressings
GMDN Term
First aid absorbent pad/bandage
Device Class
Class I
Regulation Number
880.5075
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Manufacturer details

EUDAMED SRN
DE-MF-000006024

Other devices from Hans Hepp GmbH & Co. KG

See all devices from Hans Hepp GmbH & Co. KG →

Properties

  • Sterile
  • Single Use
  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (17)

  • Implantable: No
  • Reusable: 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
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No