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Vsp

FDA UDI

Class I (US FDA UDI)

by Depuy Spine, Inc.

Identity

Trade Name
VSP FDA UDI
Generic Name
Bone tap, reusable FDA UDI
Device Name
VSP SPINE SYSTEM BONE TAP 6.25mm FDA UDI
Model / Reference
202572 FDA UDI
Description
VSP SPINE SYSTEM BONE TAP 6.25mm FDA UDI

Identifiers

Catalog Number
202572 FDA UDI
Primary DI / UDI-DI
10705034000510 FDA UDI
FDA Product Code
HWX FDA UDI
GMDN Term
Bone tap, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Vsp by Depuy Spine, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Depuy Spine, Inc.

Sources (1)

  • FDA UDI 19128156-9b2b-4d7f-a11e-07bf0090dec5 36 fields · synced May 31, 2026