← Back to catalogue

Orthofix

FDA UDI

Class I (US FDA UDI)

by Orthofix, Inc.

Identity

Trade Name
ORTHOFIX FDA UDI
Generic Name
Surgical depth gauge, reusable FDA UDI
Device Name
RODEO NAILS GAUGE D3.5 AND 4.0MM STERILE FDA UDI
Model / Reference
1 FDA UDI
Description
RODEO NAILS GAUGE D3.5 AND 4.0MM STERILE FDA UDI

Identifiers

Catalog Number
99-16730000R FDA UDI
Primary DI / UDI-DI
18059015373370 FDA UDI
FDA Product Code
FTY FDA UDI
GMDN Term
Surgical depth gauge, 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

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical depth gauge, reusable

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

Similar devices

Also classified as Surgical depth gauge, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Orthofix, Inc.

Sources (1)

  • FDA UDI 65fd55f3-755f-4be2-8200-119dae748c4e 35 fields · synced May 30, 2026