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Relief Patch for Toe

by OPPO Medical Inc.

Part of a family of 30 devices: see the family page

Ref 8007-BU-F

Relief Patch for Toe (8007-BU-F) is a Class I device made by OPPO Medical Inc., registered in EUDAMED on 12 Sep 2024 (Basic UDI-DI 08402706CL1114N) and listed in FDA GUDID since 1 Apr 2025 (UDI-DI 00840270610062), 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
United StatesGUDID listing GUDID Number00840270610062 UDI-DI Date1 Apr 2025ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number08402706CL1114N Basic UDI-DI 00840270610062UDI-DIDate12 Sep 2024RegisteredStatusActive

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08402706CL1114N registered 12 Sep 2024 Active
  • FDA GUDID UDI-DI 00840270610062 listed 1 Apr 2025 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. Registered EUDAMED 08402706CL1114N
  2. Listed FDA GUDID 00840270610062

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  • Withdrawn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
Relief Patch for Toe EUDAMED
Maxtaping GUDID
Generic name
Pressure bandage, non-latex, single-use
Device name
Tapes
Model / Ref / Catalog
8007-BU-F, 8007
Primary DI / UDI-DI
00840270610062
Basic UDI-DI
08402706CL1114N
FDA product code
KOX
EMDN code
M0599 Medical plasters - other
GMDN term
Pressure bandage, non-latex, single-use
Device class
Class I
Regulation number
878.4730
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Size
Length — 16.7 Centimeter

Manufacturer details

EUDAMED SRN
US-MF-000005202
Authorised representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Similar devices in this category

Other devices filed under MEDICAL PLASTERS - OTHER.

Other devices from OPPO Medical Inc.

See all devices from OPPO Medical Inc. →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (21, all answered No)