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Regular Tape Discs, Std, 30 pack

by Freudenberg Medical LLC

Ref BE 6041

Regular Tape Discs, Std, 30 pack (BE 6041) is a Class I device made by Freudenberg Medical LLC, registered in EUDAMED on 31 Oct 2025 (Basic UDI-DI 08482530TAPEDISCXP) and listed in FDA GUDID since 1 Jan 2018 (UDI-DI 00813307012634), active as of 22 Oct 2026.

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

CE MDR

Valid until

No date given

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

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08482530TAPEDISCXP Basic UDI-DI 00813307012634UDI-DIDate31 Oct 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number00813307012634 UDI-DI Date1 Jan 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08482530TAPEDISCXP registered 31 Oct 2025 Active
  • FDA GUDID UDI-DI 00813307012634 listed 1 Jan 2018 Listed

Certificates

0 certificates · EUDAMED

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

Timeline

2 dated events

  1. Listed FDA GUDID 00813307012634
  2. Registered EUDAMED 08482530TAPEDISCXP

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  • Withdrawn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
Regular Tape Discs, Std, 30 pack EUDAMED
InHealth Technologies; Blom-Singer GUDID
Generic name
Removable ambulatory appliance skin-adherent patch
Device name
Tapedisc
Model / reference
BE 6041
Primary DI / UDI-DI
00813307012634
Basic UDI-DI
08482530TAPEDISCXP
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 registration type
Standard device
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

Similar devices in this category

Other devices filed under RESPIRATORY AND ANESTHESIA DEVICES - ACCESSORIES NOT INCLUDED IN OTHER CLASSES.

Other devices from Freudenberg Medical LLC

See all devices from Freudenberg Medical LLC →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (20, all answered No)