← Back to catalogue

Mission

FDA UDI

Class II (US FDA UDI)

by Bard Peripheral Vascular

Identity

Trade Name
MISSION FDA UDI
Generic Name
Side-notch biopsy gun handpiece/needle FDA UDI
Device Name
Mission Disposable Core Biopsy Instrument - 16Gx10cm FDA UDI
Model / Reference
1610MS FDA UDI
Description
Mission Disposable Core Biopsy Instrument - 16Gx10cm FDA UDI

Identifiers

Catalog Number
1610MS FDA UDI
Primary DI / UDI-DI
00801741096969 FDA UDI
FDA Product Code
KNW FDA UDI
GMDN Term
Side-notch biopsy gun handpiece/needle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1075 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Needle Gauge — 16 Gauge FDA UDI
Length — 10 Centimeter FDA UDI

Category: Side-notch biopsy gun handpiece/needle

Mission by Bard Peripheral Vascular — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Side-notch biopsy gun handpiece/needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 60429ff6-97bc-419d-8cd6-d71be420bfba 36 fields · synced May 31, 2026