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Pinpoint GT 9770643

by Bard Access Systems, Inc.

Pinpoint GT 9770643 is a Class II device made by Bard Access Systems, Inc., listed in FDA GUDID since 4 Oct 2017 (UDI-DI 00801741128882), 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 Number00801741128882 UDI-DI Date4 Oct 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  • Withdrawn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
Pinpoint GT
Generic name
Hypodermic needle, single-use
Model / Ref / Catalog
9770643
Primary DI / UDI-DI
00801741128882
FDA product code
PVZ
GMDN term
Hypodermic needle, single-use
Device class
Class II
Regulation number
880.5570
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe
Size
Needle Gauge — 21 Gauge
Length — 3 Inch

Related devices

Category: Hypodermic needle, single-use

Similar devices in this category

Other devices filed under Hypodermic needle, single-use.

Other devices from Bard Access Systems, Inc.

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)