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CyberTech 900-8117

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

Ref 900-8117Model Silk Sutures

CyberTech 900-8117 is a device classified as Class IIb 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-00848782029259) and listed in FDA GUDID since 19 Feb 2019 (UDI-DI 00848782029259), 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-00848782029259 Basic UDI-DI 00848782029259UDI-DIDate29 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00848782029259 UDI-DI Date19 Feb 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00848782029259 registered 29 Oct 2026 Active
  • FDA GUDID UDI-DI 00848782029259 listed 19 Feb 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00848782029259
  2. Registered EUDAMED B-00848782029259

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  • Withdrawn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
CyberTech Silk EUDAMED
CyberTech GUDID
Generic name
Silk suture
Model / reference
900-8117, Silk Sutures
Primary DI / UDI-DI
00848782029259
Basic UDI-DI
B-00848782029259
FDA product code
GAP
EMDN code
H010202020301 Silk with needle
GMDN term
Silk suture
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
878.5030
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 IIb
GUDID
Class II

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: Silk suture

Similar devices

Also classified as Silk suture.

Similar devices in this category

Other devices filed under SILK WITH NEEDLE.

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)