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New Pentastar Medical 1276

by Bq Plus Medical Co., Ltd. 2 variants

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 Number10850067227110 UDI-DI Date30 Mar 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  • Withdrawn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
New Pentastar Medical
Generic Name
Basic intravenous administration set, noninvasive
Model / Reference
1276
Primary DI / UDI-DI
10850067227110
FDA Product Code
FPA
GMDN Term
Basic intravenous administration set, noninvasive
Device Class
Class II
Regulation Number
880.5440
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe

Other devices from Bq Plus Medical Co., Ltd.

See all devices from Bq Plus Medical Co., Ltd. →

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