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Sof-Grip Hemostat G20001

by Cook Vandergrift Inc

Ref LR-SGH001

Sof-Grip Hemostat G20001 (LR-SGH001) is a Class I device made by Cook Vandergrift Inc, registered in EUDAMED on 11 Aug 2026 (Basic UDI-DI B-00827002200012) and listed in FDA GUDID since 6 Jul 2023 (UDI-DI 00827002200012), active as of 8 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00827002200012 Basic UDI-DI 00827002200012UDI-DIDate11 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00827002200012 UDI-DI Date6 Jul 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00827002200012 registered 11 Aug 2026 Active
  • FDA GUDID UDI-DI 00827002200012 listed 6 Jul 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00827002200012
  2. Registered EUDAMED B-00827002200012

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  • Withdrawn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
Sof-Grip Hemostat
Generic name
Dressing/utility forceps, scissors-like, single-use
Device name
Lead Extraction Accessory Devices
Model / Ref / Catalog
LR-SGH001, G20001
Primary DI / UDI-DI
00827002200012
Basic UDI-DI
B-00827002200012
FDA product code
DWS
EMDN code
C0699 Cardiovascular surgery instruments, single-use - other
GMDN term
Dressing/utility forceps, scissors-like, single-use
Device class
Class I
Regulation number
870.4500
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
Model / referenceEUDAMED
LR-SGH001
GUDID
G20001

Related devices

Category: Dressing/utility forceps, scissors-like, single-use

Similar devices in this category

Other devices filed under CARDIOVASCULAR SURGERY INSTRUMENTS, SINGLE-USE - OTHER.

Other devices from Cook Vandergrift Inc

See all devices from Cook Vandergrift Inc →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (16, all answered No)