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Ultrapro UPPL6

by Johnson & Johnson International Inc.

Part of a family of 9 devices: see the family page

Ref UPPL6Model ULTRAPRO Plug

Ultrapro UPPL6 is a device classified as Class III in the EU and Class II in the US made by Johnson & Johnson International Inc., registered in EUDAMED on 19 Jul 2025 (Basic UDI-DI 0705031a011524G) and listed in FDA GUDID since 1 Sep 2015 (UDI-DI 10705031132580), active as of 7 Nov 2026.

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

CE MDR

Valid until

3 Dec 2030

CE MDR certificate

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

1 certificate

Certifier BSI Group The Netherlands B.V.

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0705031a011524G Basic UDI-DI 10705031132580UDI-DIDate19 Jul 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number10705031132580 UDI-DI Date1 Sep 2015ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0705031a011524G registered 19 Jul 2025 Active
  • FDA GUDID UDI-DI 10705031132580 listed 1 Sep 2015 Listed

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • MDR 730048 Active Reissued

    Technical documentation EU MDR

    Certifier
    BSI Group The Netherlands B.V. 2797
    Issued
    4 Dec 2025
    Expires
    3 Dec 2030

Timeline

2 dated events

  1. Listed FDA GUDID 10705031132580
  2. Registered EUDAMED 0705031a011524G

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  • Withdrawn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
Ultrapro
Generic name
Extra-gynaecological surgical mesh, composite-polymer
Device name
ULTRAPRO Plug
Model / Ref / Catalog
UPPL6, ULTRAPRO Plug
Primary DI / UDI-DI
10705031132580
Basic UDI-DI
0705031a011524G
FDA product code
FTL
EMDN code
P900204 Surgical meshes, more than one component
GMDN term
Extra-gynaecological surgical mesh, composite-polymer
Device class
Class III EUDAMED
Class II GUDID
Regulation number
878.3300
EU registration type
Standard device
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class III
GUDID
Class II

Device class is stated on each registry's own scale: Class III in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Extra-gynaecological surgical mesh, composite-polymer

Similar devices in this category

Other devices filed under SURGICAL MESHES, MORE THAN ONE COMPONENT.

Other devices from Johnson & Johnson International Inc.

See all devices from Johnson & Johnson International Inc. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)