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Truguide

FDA UDI

Class II (US FDA UDI)

by Bard Peripheral Vascular

Identity

Trade Name
TRUGUIDE FDA UDI
Generic Name
Needle guide, single-use FDA UDI
Device Name
TRUGUIDE® Disposable Coaxial Biopsy Needle with Depth Stop, 15g x 17.8cm FDA UDI
Model / Reference
C1620A FDA UDI
Description
TRUGUIDE® Disposable Coaxial Biopsy Needle with Depth Stop, 15g x 17.8cm FDA UDI

Identifiers

Catalog Number
C1620A FDA UDI
Primary DI / UDI-DI
00801741084980 FDA UDI
FDA Product Code
FCG FDA UDI
GMDN Term
Needle guide, single-use 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 — 15 Gauge FDA UDI
Length — 17.8 Centimeter FDA UDI

Category: Needle guide, single-use

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

Similar devices

Also classified as Needle guide, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b777b6ca-6edf-4391-a006-106a01e09750 36 fields · synced May 30, 2026