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PowerMidline CK001098

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 Number00801741240904 UDI-DI Date27 Aug 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  • Withdrawn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
PowerMidline
Generic Name
Peripheral vascular intervention infusion catheter
Model / Ref / Catalog
CK001098
Primary DI / UDI-DI
00801741240904
FDA Product Code
PND
GMDN Term
Peripheral vascular intervention infusion catheter
Device Class
Class II
Regulation Number
880.5200
GUDID distribution status
In Commercial Distribution
Size
Catheter Gauge — 4 French
Length — 20 Centimeter

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Properties

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

Other properties (7)

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