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D.B.S. Dynamic Brace System

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref DBS1Model M:DBS1 // R:DE/CA09/0760/2 32

by Meditrac Ltd.

Identity

Trade Name
D.B.S. EUDAMED
D.B.S. Dynamic Brace System FDA UDI
Generic Name
Wearable lumbar spine traction device FDA UDI
Device Name
Dynamic Brace System (DBS) EUDAMED
The DBS (Dynamic Brace System) is an accessory to the Vertetrac, intended for the treatment of scoliosis. Idiopathic scoliosis (juvenile, adolescent, or adult) FDA UDI
Model / Reference
DBS1 EUDAMEDFDA UDI
M:DBS1 // R:DE/CA09/0760/2 32 EUDAMED
Description
The DBS (Dynamic Brace System) is an accessory to the Vertetrac, intended for the treatment of scoliosis. Idiopathic scoliosis (juvenile, adolescent, or adult) FDA UDI

Identifiers

Primary DI / UDI-DI
07290015711302 EUDAMEDFDA UDI
Basic UDI-DI
7290015711D.B.S.H6 EUDAMED
Direct Marketing DI
07290015711302 EUDAMED
FDA Product Code
KQZ FDA UDI
EMDN Code
Z12130202 TRACTION SYSTEMS EUDAMED
GMDN Term
Wearable lumbar spine traction device FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.5890 FDA UDI
Market of Registration
Spain EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wearable lumbar spine traction device

D.B.S. Dynamic Brace System by Meditrac Ltd. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Wearable lumbar spine traction device.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Meditrac Ltd.

Sources (2)

  • FDA UDI 2dd1b5bd-c42e-4696-bf8b-5f8b502ace14 33 fields · synced Jul 28, 2026
  • EUDAMED 5543d8b5-9294-4e2d-a30c-8cb425bbf89a 61 fields · synced Jul 28, 2026