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ManaMed

FDA UDI

Class I (US FDA UDI)

by Manamed Llc

Identity

Trade Name
ManaMed FDA UDI
Generic Name
Knee support orthosis FDA UDI
Device Name
The Cabo (formerly Trailblazer) is one of the lightest double upright braces on the market. This innovative system features an aluminum alloy frame with a proprietary quick fitting magnetic buckle system. Lightweight and low-profile Magnetic quick releasing buckles Pivoting condyle pads for an optimal fit Step through design FDA UDI
Model / Reference
Cabo Knee Medium Right FDA UDI
Description
The Cabo (formerly Trailblazer) is one of the lightest double upright braces on the market. This innovative system features an aluminum alloy frame with a proprietary quick fitting magnetic buckle system. Lightweight and low-profile Magnetic quick releasing buckles Pivoting condyle pads for an optimal fit Step through design FDA UDI

Identifiers

Catalog Number
TRBL45M1 FDA UDI
Primary DI / UDI-DI
00810113680033 FDA UDI
FDA Product Code
ITQ FDA UDI
GMDN Term
Knee support orthosis FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3475 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Knee support orthosis

ManaMed by Manamed Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Knee support orthosis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Manamed Llc

Sources (1)

  • FDA UDI 8b84148a-8656-4e39-bc36-e186123c6bee 35 fields · synced Jun 1, 2026