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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
Orthopaedic chisel FDA UDI
Device Name
EXCAVATOR WITH HOLE DOUBLE ENDED 1.5MM / 2.5MM 5.75" FDA UDI
Model / Reference
75430-13 FDA UDI
Description
EXCAVATOR WITH HOLE DOUBLE ENDED 1.5MM / 2.5MM 5.75" FDA UDI

Identifiers

Primary DI / UDI-DI
00810158210158 FDA UDI
FDA Product Code
FHL FDA UDI
GMDN Term
Orthopaedic chisel FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4730 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic chisel

Princeton by Princeton Medical Group, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic chisel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Princeton Medical Group, Inc.

Sources (1)

  • FDA UDI a86423de-9d48-4a43-9dd6-56dcb6379602 33 fields · synced May 30, 2026