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Gammapro Angled

by General Equipment for Medical Imaging SA

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

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

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08437018413294 UDI-DI Date18 Jan 2023ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Gammapro
Generic Name
Intraoperative gamma radiation detection system probe, reusable
Model / Ref / Catalog
ANGLED, IC-1180
Primary DI / UDI-DI
08437018413294
FDA Product Code
IZD
GMDN Term
Intraoperative gamma radiation detection system probe, reusable
Device Class
Class I
Regulation Number
892.1320
GUDID distribution status
In Commercial Distribution
Sterilization Method
Hydrogen Peroxide
Size
Length — 259 Millimeter
Weight — 122 Gram
Width — 40 Millimeter
Height — 40 Millimeter

Related devices

Category: Intraoperative gamma radiation detection system probe, reusable

Properties

  • Prescription Use
  • Combination Product
  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No