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Princeton

FDA UDI

Class I (US FDA UDI)

by Princeton Medical Group, Inc.

Identity

Trade Name
PRINCETON FDA UDI
Generic Name
Percussion hammer, manual, reusable FDA UDI
Device Name
MALLET 1 INTERCHANGEABLE PLASTIC DISC 26MMØ 240G (.53LBS) 7.5" FDA UDI
Model / Reference
33694-24 FDA UDI
Description
MALLET 1 INTERCHANGEABLE PLASTIC DISC 26MMØ 240G (.53LBS) 7.5" FDA UDI

Identifiers

Primary DI / UDI-DI
00810158212343 FDA UDI
FDA Product Code
HXL FDA UDI
GMDN Term
Percussion hammer, manual, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

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

Princeton by Princeton Medical Group, 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

Sources (1)

  • FDA UDI f4a62dd9-9fdd-49fa-91cc-10e4c595b5ed 33 fields · synced Jun 1, 2026