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McKesson

FDA UDI

Class I (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name
McKesson FDA UDI
Generic Name
Percussion hammer, manual, reusable FDA UDI
Device Name
Hammer, Babinski Percussion, Adult, OG FDA UDI
Model / Reference
43-2-012 FDA UDI
Description
Hammer, Babinski Percussion, Adult, OG FDA UDI

Identifiers

Primary DI / UDI-DI
00612479198890 FDA UDI
FDA Product Code
GWZ FDA UDI
GMDN Term
Percussion hammer, manual, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.1700 FDA UDI
Commercial Distribution
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

Category: Percussion hammer, manual, reusable

McKesson by Mckesson Medical-Surgical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Percussion hammer, manual, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mckesson Medical-Surgical Inc.

Sources (1)

  • FDA UDI 33ab1b5e-83dd-4c65-80cf-69db30155856 33 fields · synced May 31, 2026