gudid
Primary ID: 1204-610 U M
WELLBRACE (UDI 1204-610 U M)
Manufactured by PANTYMED S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for WELLBRACE - Primary ID 1204-610 U M
Device Regulatory Overview
The WELLBRACE (Model/Catalog Number: 1204-610 U M) is a medical device manufactured by PANTYMED S.A.. This product is indexed under FDA Product Code / Category Classification IPT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1204-610 U M
- Product Code / EMDN
- IPT
- Device Name
- FAJA TORACICA MASCULINA- WELLB U M
- Database Sync Date
- 2026-08-09 09:07:23
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of WELLBRACE?
The registered manufacturer of record for WELLBRACE is PANTYMED S.A..
What is the Primary UDI-DI identifier for WELLBRACE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1204-610 U M.
What classification code is assigned to this device?
This device is registered under product classification code IPT.
Similar Classification Devices (IPT)
Other Devices by PANTYMED S.A.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint