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Gantry Guard Flex Mini CTG03

by Precision Dynamics Corporation

Gantry Guard Flex Mini CTG03 is a Class II device made by Precision Dynamics Corporation, listed in FDA GUDID since 25 Apr 2018 (UDI-DI 10687225677865), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10687225677865 UDI-DI Date25 Apr 2018ListedStatusListed GUDID: not in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Gantry Guard Flex Mini
Generic name
Medical equipment/instrument drape, single-use
Model / Ref / Catalog
CTG03
Primary DI / UDI-DI
10687225677865
FDA product code
PUI
GMDN term
Medical equipment/instrument drape, single-use
Device class
Class II
Regulation number
878.4370
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code PUI (Drape, Surgical, Exempt).

Other devices from Precision Dynamics Corporation

See all devices from Precision Dynamics Corporation →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)