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Monopty 121416

by Bard Peripheral Vascular

Monopty 121416 is a Class II device made by Bard Peripheral Vascular, listed in FDA GUDID since 12 Sep 2016 (UDI-DI 00801741084591), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00801741084591 UDI-DI Date12 Sep 2016ListedStatusListed 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  • Withdrawn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
Monopty
Generic name
Side-notch biopsy gun handpiece/needle
Model / Ref / Catalog
121416
Primary DI / UDI-DI
00801741084591
FDA product code
KNW
GMDN term
Side-notch biopsy gun handpiece/needle
Device class
Class II
Regulation number
876.1075
GUDID distribution status
In Commercial Distribution
Size
Needle Gauge — 14 Gauge
Length — 16 Centimeter

Related devices

Category: Side-notch biopsy gun handpiece/needle

Similar devices in this category

Other devices filed under Side-notch biopsy gun handpiece/needle.

Other devices from Bard Peripheral Vascular

See all devices from Bard Peripheral Vascular →

Properties

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