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Arrow IPN922101

by Teleflex Incorporated

Ref 9066-VC-005Model IPN922101

Arrow IPN922101 (9066-VC-005) is a Class I device made by Teleflex Incorporated, registered in EUDAMED on 25 May 2026 (Basic UDI-DI B-10816000013868) and listed in FDA GUDID since 4 Apr 2025 (UDI-DI 10816000013868), active as of 23 Oct 2026.

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

CE MDD

Valid until

No date given

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

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10816000013868 Basic UDI-DI 10816000013868UDI-DIDate25 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10816000013868 UDI-DI Date4 Apr 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10816000013868 registered 25 May 2026 Active
  • FDA GUDID UDI-DI 10816000013868 listed 4 Apr 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10816000013868
  2. Registered EUDAMED B-10816000013868

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
EZ-Stabilizer EUDAMED
Arrow GUDID
Generic name
Dressing-fixation skin adhesive tape, non-silicone
Device name
Ez-Stabilizer(Box of 5)
Model / Ref / Catalog
IPN922101, 9066-VC-005
Primary DI / UDI-DI
10816000013868
Basic UDI-DI
B-10816000013868
FDA product code
KMK
EMDN code
M04010299 Fixing dressings - other
GMDN term
Dressing-fixation skin adhesive tape, non-silicone
Device class
Class I
Regulation number
880.5210
EU registration type
Legacy device (under a directive)
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under FIXING DRESSINGS - OTHER.

Other devices from Teleflex Incorporated

  • Arrow IPNB00820 Open recall

    Class II
  • Arrow IPNB00826 Open recall

    Class II
  • Arrow IPNB00822 Open recall

    Class II
  • Arrow IPNB00827 Open recall

    Class II

See all devices from Teleflex Incorporated →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (18, all answered No)