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Permatape 223165

by Medos International Sàrl

Ref 223165

Permatape 223165 is a device classified as Class IIb in the EU and Class II in the US made by Medos International Sàrl, registered in EUDAMED on 22 Sep 2026 (Basic UDI-DI B-CHMF000014268000017Y8) and listed in FDA GUDID since 17 Feb 2017 (UDI-DI D-CHMF000014268000017Y8), 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-CHMF000014268000017Y8 Basic UDI-DI D-CHMF000014268000017Y8UDI-DIDate22 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberD-CHMF000014268000017Y8 UDI-DI Date17 Feb 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-CHMF000014268000017Y8 registered 22 Sep 2026 Active
  • FDA GUDID UDI-DI D-CHMF000014268000017Y8 listed 17 Feb 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID D-CHMF000014268000017Y8
  2. Registered EUDAMED B-CHMF000014268000017Y8

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  • Withdrawn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
Permatape
Generic name
Polyolefin/fluoropolymer suture, multifilament
Model / Ref / Catalog
223165
Primary DI / UDI-DI
D-CHMF000014268000017Y8 EUDAMED
10886705027859 GUDID
Basic UDI-DI
B-CHMF000014268000017Y8
FDA product code
GAT
EMDN code
H0102010299 Synthetic nonabsorbable multifilament sutures - other
GMDN term
Polyolefin/fluoropolymer suture, multifilament
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
878.5000
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
D-CHMF000014268000017Y8
GUDID
10886705027859
Device classEUDAMED
Class IIb
GUDID
Class II

The registries describe this device under different primary UDI-DIs (EUDAMED lists D-CHMF000014268000017Y8; FDA GUDID lists 10886705027859), so their flags are not compared. Device class is stated on each registry's own scale: Class IIb 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: Polyolefin/fluoropolymer suture, multifilament

Similar devices in this category

Other devices filed under SYNTHETIC NONABSORBABLE MULTIFILAMENT SUTURES - OTHER.

Other devices from Medos International SARL

See all devices from Medos International SARL →

Properties

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