Belpro Medical Inc.

FDA UDI

Class II (US FDA UDI)

by Belpro Medical Inc.

Identity

Trade Name: Belpro Medical Inc. FDA UDI
Generic Name: Biopsy syringe holder, reusable FDA UDI
Device Name: Biopsy syringe holder, 20cc, stainless steel, reusable FDA UDI
Model / Reference: 920 FDA UDI
Description: Biopsy syringe holder, 20cc, stainless steel, reusable FDA UDI

Identifiers

Catalog Number: 920 FDA UDI
Primary DI / UDI-DI: 00807355100238 FDA UDI
FDA Product Code: KNW FDA UDI
GMDN Term: Biopsy syringe holder, reusable 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Liquid Chemical FDA UDI

Category: Biopsy syringe holder, reusable

Belpro Medical Inc. by Belpro Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Belpro Medical Inc — Belpro Medical Inc. · Class II
Belpro Medical Inc. — Belpro Medical Inc. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Belpro Medical Inc.

Sources (1)

FDA UDI b481d8e4-407d-4202-91ea-583bace0fa09 34 fields · synced Jun 8, 2026