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Rhino

FDA UDI

Class I (US FDA UDI)

by MD Orthopaedics

Identity

Trade Name
Rhino FDA UDI
Generic Name
Cast boot FDA UDI
Device Name
Cast Boot 5 1/2 FDA UDI
Model / Reference
Cast Boot 5 1/2 FDA UDI
Description
Cast Boot 5 1/2 FDA UDI

Identifiers

Catalog Number
99 FDA UDI
Primary DI / UDI-DI
00810060883488 FDA UDI
FDA Product Code
IPG FDA UDI
GMDN Term
Cast boot FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3025 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

Yes

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: Cast boot

Rhino by MD Orthopaedics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cast boot.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
MD Orthopaedics

Sources (1)

  • FDA UDI c8fdbdca-68cb-4c82-a8d1-a582a73f3884 34 fields · synced May 30, 2026