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Wellbrace

FDA UDI

Class I (US FDA UDI)

by Pantymed S.a.

Identity

Trade Name
WELLBRACE FDA UDI
Generic Name
Clavicle orthosis FDA UDI
Device Name
CORRECTOR DE POSTURA DE NEOPRE - M FDA UDI
Model / Reference
1203-E1 U M FDA UDI
Description
CORRECTOR DE POSTURA DE NEOPRE - M FDA UDI

Identifiers

Primary DI / UDI-DI
07798094545936 FDA UDI
FDA Product Code
IPT FDA UDI
GMDN Term
Clavicle 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

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Clavicle orthosis

Wellbrace by Pantymed S.a. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Clavicle orthosis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pantymed S.a.

Sources (1)

  • FDA UDI 17c7f2d9-5330-4a00-9ac9-ded53fb0d4a7 33 fields · synced Jun 8, 2026