Skip to content

Xpress BCD LLC Inner Pack

by Xpress Bcd LLC

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860008878335 UDI-DI Date5 May 2023ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Xpress BCD LLC
Generic Name
Radiological breast positioner haemostatic compression attachment
Model / Reference
Inner Pack
Primary DI / UDI-DI
00860008878335
510(k) Number
FDA Product Code
POY
GMDN Term
Radiological breast positioner haemostatic compression attachment
Device Class
Class II
Regulation Number
892.1710
GUDID distribution status
In Commercial Distribution

Related devices

Category: Radiological breast positioner haemostatic compression attachment

Cleared under the same submission (K163388)

Other devices from Xpress Bcd LLC

Properties

  • Prescription Use
  • Lot / Batch Number

Other properties (12)

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