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PowerLoc 0672034J

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 Number00801741151477 UDI-DI Date12 Jan 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  • Withdrawn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
PowerLoc
Generic Name
Vascular port administration set
Model / Ref / Catalog
0672034J
Primary DI / UDI-DI
00801741151477
FDA Product Code
FPA
GMDN Term
Vascular port administration set
Device Class
Class II
Regulation Number
880.5440
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional
Size
Length — 0.75 Inch
Needle Gauge — 20 Gauge

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

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