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Deknatel IPN923603

by Teleflex Incorporated

Ref EGFS-10A

Deknatel IPN923603 (EGFS-10A) is a Class I device made by Teleflex Incorporated, registered in EUDAMED on 6 Aug 2026 (Basic UDI-DI 08019020000000000000156KQ) and listed in FDA GUDID since 4 Sep 2025 (UDI-DI 14026704738998), active as of 23 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 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/MDR EUDAMED Number08019020000000000000156KQ Basic UDI-DI 14026704738998UDI-DIDate6 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number14026704738998 UDI-DI Date4 Sep 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08019020000000000000156KQ registered 6 Aug 2026 Active
  • FDA GUDID UDI-DI 14026704738998 listed 4 Sep 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 14026704738998
  2. Registered EUDAMED 08019020000000000000156KQ

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  • Withdrawn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
Gabbay-Frater Sutorganizer (4 Pcs of 3) EUDAMED
Deknatel GUDID
Generic name
Polyester suture, non-bioabsorbable, multifilament, non-antimicrobial
Device name
Gabbay-Frater Suture Guide
Model / Ref / Catalog
EGFS-10A, IPN923603
Primary DI / UDI-DI
14026704738998
Basic UDI-DI
08019020000000000000156KQ
Unit of use DI
24026704738995
FDA product code
FZX
EMDN code
H9099 Suture devices - other
GMDN term
Polyester suture, non-bioabsorbable, multifilament, non-antimicrobial
Device class
Class I
Regulation number
878.4800
EU registration type
Standard device
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution
Size
Width — 1.5 Inch
Length — 9 Inch
Depth — 0.75 Inch

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
EGFS-10A
GUDID
IPN923603
ImplantableEUDAMED
No
GUDID
Yes

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Properties

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