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PowerPICC Provena CK000993B

by Bard Access Systems, Inc.

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00801741237218 UDI-DI Date7 Oct 2025ListedStatusListed 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  • Withdrawn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
PowerPICC Provena
Generic Name
Peripherally-inserted central venous catheter
Model / Ref / Catalog
CK000993B
Primary DI / UDI-DI
00801741237218
FDA Product Code
LJS
GMDN Term
Peripherally-inserted central venous catheter
Device Class
Class II
Regulation Number
880.5970
GUDID distribution status
In Commercial Distribution
Size
Catheter Gauge — 5 French
Length — 55 Centimeter

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Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Convenience Kit
  • Combination Product
  • Lot / Batch Number
  • Expiration Date

Other properties (6)

  • Contains Latex: No
  • Over-the-Counter: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No