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TM "Rehabilitimed" DS-1 UNI Comfort

FDA UDI

Class I (US FDA UDI)

by Reabilitimed Tov

Identity

Trade Name
TM "Rehabilitimed" DS-1 UNI Comfort FDA UDI
Generic Name
Ankle/foot orthosis FDA UDI
Device Name
It has the appearance of an open structure in the form of a boot, to which a transverse crossbar is attached, which prevents rotation of the foot and the entire leg to the right, left, and additional fixing straps keep the foot from bending movements up and down. Beige color. FDA UDI
Model / Reference
DS-1 UNI Comfort FDA UDI
Description
It has the appearance of an open structure in the form of a boot, to which a transverse crossbar is attached, which prevents rotation of the foot and the entire leg to the right, left, and additional fixing straps keep the foot from bending movements up and down. Beige color. FDA UDI

Identifiers

Catalog Number
DS-1 UNI Comfort FDA UDI
Primary DI / UDI-DI
04823097716847 FDA UDI
FDA Product Code
ITW FDA UDI
GMDN Term
Ankle/foot 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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: Ankle/foot orthosis

TM "Rehabilitimed" DS-1 UNI Comfort by Reabilitimed Tov — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ankle/foot orthosis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Reabilitimed Tov

Sources (1)

  • FDA UDI 89ef4288-0ce7-4efa-b84d-4b7f977f8c91 35 fields · synced May 30, 2026