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TM "Rehabilitimed" OT-1V Mp Comfort

FDA UDI

Class I (US FDA UDI)

by Reabilitimed Tov

Identity

Trade Name
TM "Rehabilitimed" OT-1V Mp Comfort FDA UDI
Generic Name
Thoracic spine orthosis FDA UDI
Device Name
The beige posture corrector provides an average degree of fixation due to 2 modeled duralumin stiffening ribs. Designed to form the correct posture and correct existing defects. Correction of spinal deformity is carried out in stages in 2-3 techniques by gradually changing the degree of tension of the straps. Made of durable elastic bandage fabric made of polyamide and elastane and multilayer material with a cotton layer to the body and polyamide on the outside. FDA UDI
Model / Reference
OT-1V Mp Comfort FDA UDI
Description
The beige posture corrector provides an average degree of fixation due to 2 modeled duralumin stiffening ribs. Designed to form the correct posture and correct existing defects. Correction of spinal deformity is carried out in stages in 2-3 techniques by gradually changing the degree of tension of the straps. Made of durable elastic bandage fabric made of polyamide and elastane and multilayer material with a cotton layer to the body and polyamide on the outside. FDA UDI

Identifiers

Catalog Number
OT-1V Mp Comfort FDA UDI
Primary DI / UDI-DI
04823097722114 FDA UDI
FDA Product Code
IPT FDA UDI
GMDN Term
Thoracic spine orthosis FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3490 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: Thoracic spine orthosis

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

Similar devices

Also classified as Thoracic spine 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 8753c26d-68e5-4a61-bfe5-af7e52fffca9 36 fields · synced May 30, 2026