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Bleed ID Suction Pad

by Aparata Medical

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 NumberG8057116571 UDI-DI Date2 Mar 2026ListedStatusListed 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  • Withdrawn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
Bleed ID
Generic Name
Blood loss estimation suction pad
Model / Ref / Catalog
Suction Pad, 711657
Primary DI / UDI-DI
G8057116571
FDA Product Code
GCX
GMDN Term
Blood loss estimation suction pad
Device Class
Class II
Regulation Number
880.6740
GUDID distribution status
In Commercial Distribution
Size
Length — 32 Inch
Width — 32 Inch

Other devices from Aparata Medical

Properties

  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No