Bone Cement Gouge, Outside Bevelled, 10MM x 310MM

FDA UDI

Class I (US FDA UDI)

by Biopro, Inc.

Identity

Trade Name: Bone Cement Gouge, Outside Bevelled, 10MM x 310MM FDA UDI
Generic Name: Surgical gouge FDA UDI
Model / Reference: 95-7180 FDA UDI

Identifiers

Primary DI / UDI-DI: 00810012485050 FDA UDI
FDA Product Code: HWJ FDA UDI
GMDN Term: Surgical gouge FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4540 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Category: Surgical gouge

Bone Cement Gouge, Outside Bevelled, 10MM x 310MM by Biopro, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 I	Pending data

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Manufacturer

Manufacturer: Biopro, Inc.

Sources (1)

FDA UDI 224c7a8c-443a-4d2c-b964-16cb70c16e99 32 fields · synced May 31, 2026