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Life PRP LLC 24BC12ml

by Life Prp

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 Number00199874715100 UDI-DI Date30 May 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  • Withdrawn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
Life PRP LLC
Generic Name
Evacuated blood collection tube IVD, anticoagulant/separator
Model / Reference
24BC12ml
Primary DI / UDI-DI
00199874715100
FDA Product Code
KST
GMDN Term
Evacuated blood collection tube IVD, anticoagulant/separator
Device Class
Class I
Regulation Number
864.9125
GUDID distribution status
In Commercial Distribution

Other devices from Life Prp

Properties

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

Other properties (8)

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