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MatrixMANDIBLE

FDA UDI

Class I (US FDA UDI)

by Synthes

Identity

Trade Name
MatrixMANDIBLE FDA UDI
Generic Name
Orthopaedic implantable-device cutter FDA UDI
Device Name
MATRIXMANDIBLE SHORT CUT PLATE CUTTER FDA UDI
Model / Reference
03.503.057 FDA UDI
Description
MATRIXMANDIBLE SHORT CUT PLATE CUTTER FDA UDI

Identifiers

Catalog Number
03503057 FDA UDI
Primary DI / UDI-DI
10887587011783 FDA UDI
FDA Product Code
HTZ FDA UDI
GMDN Term
Orthopaedic implantable-device cutter 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

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: Orthopaedic implantable-device cutter

MatrixMANDIBLE by Synthes — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implantable-device cutter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Synthes

Sources (1)

  • FDA UDI 72f05e2c-ccc4-487b-a24d-4f93b6e142c6 35 fields · synced Jun 1, 2026