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Fumedica H26-2723C

by Surgical Specialties México, S. de R.L. de C.V.

Ref H26-2723CModel Polyester Sutures

Fumedica H26-2723C is a device classified as Class III in the EU and Class II in the US made by Surgical Specialties México, S. de R.L. de C.V., registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI B-00848782042807) and listed in FDA GUDID since 22 Oct 2021 (UDI-DI 00848782042807), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00848782042807 Basic UDI-DI 00848782042807UDI-DIDate29 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00848782042807 UDI-DI Date22 Oct 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00848782042807 registered 29 Oct 2026 Active
  • FDA GUDID UDI-DI 00848782042807 listed 22 Oct 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00848782042807
  2. Registered EUDAMED B-00848782042807

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  • Withdrawn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
FSSB Polyester EUDAMED
Fumedica GUDID
Generic name
Polyester suture, non-bioabsorbable, multifilament, non-antimicrobial
Model / Ref / Catalog
H26-2723C, Polyester Sutures
Primary DI / UDI-DI
00848782042807
Basic UDI-DI
B-00848782042807
FDA product code
GAT
EMDN code
H010201010201 Polyester and derivatives monofilament with needle
GMDN term
Polyester suture, non-bioabsorbable, multifilament, non-antimicrobial
Device class
Class III EUDAMED
Class II GUDID
Regulation number
878.5000
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

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: Polyester suture, non-bioabsorbable, multifilament

Similar devices in this category

Other devices filed under MONOFILAMENT NON-ABSORBABLE SYNTHETIC SUTURES.

Other devices from Surgical Specialties México, S. de R.L. de C.V.

See all devices from Surgical Specialties México, S. de R.L. de C.V. →

Properties

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