gudid
Primary ID: 1207-F1 U XL
WELLBRACE (UDI 1207-F1 U XL)
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 1207-F1 U XL
Device Regulatory Overview
The WELLBRACE (Model/Catalog Number: 1207-F1 U XL) is a medical device manufactured by PANTYMED S.A.. This product is indexed under FDA Product Code / Category Classification IPY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1207-F1 U XL
- Product Code / EMDN
- IPY
- Device Name
- FAJA SACROLUMBAR NEOPRENE - PR U XL
- Database Sync Date
- 2026-08-09 09:07:23
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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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 1207-F1 U XL.
What classification code is assigned to this device?
This device is registered under product classification code IPY.
Similar Classification Devices (IPY)
Other Devices by PANTYMED S.A.
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