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C-Arm Cover 07-CA220

by Advance Medical Designs, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None ongoing

1 closed

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 Number00848340013065 UDI-DIDate26 Feb 2024ListedStatusListed GUDID: in commercial distribution

Recalls

1 recall · FDA

    • Terminated Z-1036-04 FDA Unclassified (pre-2012) initiated 18 Jun 2004

    The product may come apart when excessive force is applied to the coupler.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
C-Arm Cover
Generic Name
Medical equipment/instrument drape, single-use
Model / Reference
07-CA220
Primary DI / UDI-DI
00848340013065
510(k) Number
FDA Product Code
JAA
GMDN Term
Medical equipment/instrument drape, single-use
Device Class
Class II
Regulation Number
892.1650
GUDID distribution status
In Commercial Distribution
Sterilization Method
Ethylene Oxide

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Properties

  • Single Use
  • Lot / Batch Number
  • Expiration Date

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No