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Lone Star 3302G

by CooperSurgical, Inc.

Ref 3302GModel 3707

Active European Union. Also listed in GUDID (US).

CE MDR CE MDD

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0888937TD007sYJ Basic UDI-DI 00888937015355UDI-DIDate15 Sep 2025RegisteredStatusActive
European UnionCE/MDD EUDAMED Number0888937TD007sYJ Basic UDI-DI 00888937015355UDI-DIDate15 Sep 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number00888937015355 UDI-DI Date30 Oct 2022ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR, CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Lone Star® EUDAMED
Lone Star GUDID
Generic Name
Surgical retraction system mounting frame, single-use
Device Name
Lone Star® Retractor System™
Lone Star® Retractors (Sterile)
Model / Reference
3302G, 3707
Primary DI / UDI-DI
00888937015355
Basic UDI-DI
0888937TD007sYJ, B-00888937015355
FDA Product Code
GAD
EMDN Code
V9012 Non-specialist surgical instruments and kits, single-use
GMDN Term
Surgical retraction system mounting frame, single-use
Device Class
Class I EUDAMEDGUDID
Class IIa EUDAMED
Regulation Number
878.4800
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 22 Centimeter
Outer Diameter — 11.3 Centimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class I
Class IIa
GUDID
Class I

Other devices from CooperSurgical, Inc.

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (19)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No