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ASP Global / Primo CF120B

by Asp Global, LLC

ASP Global / Primo CF120B is a Class II device made by Asp Global, LLC, listed in FDA GUDID since 4 Sep 2026 (UDI-DI 00840216128774), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00840216128774 UDI-DI Date4 Sep 2026ListedStatusListed GUDID: 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  • Withdrawn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
ASP Global / Primo
Generic name
Patient transfer/turning sheet, single-use
Model / reference
CF120B
Primary DI / UDI-DI
00840216128774
FDA product code
FRZ
GMDN term
Patient transfer/turning sheet, single-use
Device class
Class II
Regulation number
880.6775
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FRZ (Device, Patient Transfer, Powered).

Other devices from Asp Global, LLC

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Properties

  • Premarket exempt
  • Lot / batch number
  • Serial number
Other properties (12, all answered No)