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Thin Adhesive Tape Discs, Standard, 30 pack

by Freudenberg Medical LLC

Ref BE 6043

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

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None, self-declared

Class I: no certifier involved

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/MDR EUDAMED Number08482530THINTAPEDISC36 Basic UDI-DI 00813307012658UDI-DIDate31 Oct 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number00813307012658 UDI-DI Date1 Jan 2018ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade Name
Thin Adhesive Tape Discs, Standard, 30 pack EUDAMED
InHealth Technologies; Blom-Singer GUDID
Generic Name
Removable ambulatory appliance skin-adherent patch
Device Name
Thintapedisc
Model / Reference
BE 6043
Primary DI / UDI-DI
00813307012658
Basic UDI-DI
08482530THINTAPEDISC36
FDA Product Code
KGX
EMDN Code
R9080 Respiratory and anesthesia devices - accessories not included in other classes
GMDN Term
Removable ambulatory appliance skin-adherent patch
Device Class
Class I
Regulation Number
880.5240
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Manufacturer details

EUDAMED SRN
US-MF-000023823
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Related devices

Category: Gas-sampling/monitoring respiratory tubing, single-use

Other devices from Freudenberg Medical LLC

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Properties

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

Other properties (19)

  • Sterile: No
  • 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
  • Manufacturing Date: No