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J-Vac

by Ethicon, Inc. 6 variants

Ref 2199Model J-VAC Adapter

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0705031a020534L Basic UDI-DI 10705031003422UDI-DIDate14 Jan 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10705031003422 UDI-DI Date23 Sep 2015ListedStatusListed GUDID: in commercial distribution

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  • Withdrawn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 Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Generic Name
Closed-wound drain, non-bioabsorbable
Device Name
J-VAC Closed Wound Drainage Products and Accessories (Including BLAKE Drains)
Model / Ref / Catalog
J-VAC Adapter, 2199
Primary DI / UDI-DI
10705031003422
Basic UDI-DI
0705031a020534L
FDA Product Code
GBX
EMDN Code
A070199 Adapters and connectors - other
GMDN Term
Closed-wound drain, non-bioabsorbable
Device Class
Class I
Regulation Number
878.4200
Market of Registration
Belgium
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Contains LatexEUDAMED
No
GUDID
Yes

Manufacturer details

EUDAMED SRN
US-MF-000013113
Authorised representative
Johnson & Johnson Medical GmbH DE-AR-000007712

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Properties

  • Sterile
  • Single Use
  • Contains Latex NoEUDAMEDYesGUDID
  • Endocrine Disruptor
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (16)

  • Implantable: No
  • Reusable: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No