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Patella Calliper

FDA UDI

Class I (US FDA UDI)

by Signature Orthopaedics Pty Ltd

Identity

Trade Name
Patella Calliper FDA UDI
Generic Name
Medical ruler, reusable FDA UDI
Model / Reference
02-039-90-5000 FDA UDI

Identifiers

Primary DI / UDI-DI
09348215098667 FDA UDI
FDA Product Code
FTY FDA UDI
GMDN Term
Medical ruler, 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

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Medical ruler, reusable

Patella Calliper by Signature Orthopaedics Pty Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical ruler, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 29fc5c82-4e3d-43d2-aa3b-edb28b98a03d 32 fields · synced May 30, 2026