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PowerMidline CK000773

by Bard Access Systems, Inc.

PowerMidline CK000773 is a Class II device made by Bard Access Systems, Inc., listed in FDA GUDID since 16 Aug 2017 (UDI-DI 00801741142499), registry data as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00801741142499 UDI-DI Date16 Aug 2017ListedStatusListed GUDID: in commercial distribution

Official records

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  • Withdrawn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
CK000773
Primary DI / UDI-DI
00801741142499
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
Length — 20 Centimeter
Catheter Gauge — 4 French

Related devices

Category: Peripheral vascular intervention infusion catheter

Similar devices in this category

Other devices filed under Peripheral vascular intervention infusion catheter.

Other devices from Bard Access Systems, Inc.

See all devices from Bard Access Systems, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)