eudamed_udi
Primary ID: 08904085093631
Bayflex (UDI 08904085093631)
Manufactured by EUCARE PHARMACEUTICALS PRIVATE LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bayflex - Primary ID 08904085093631
Device Regulatory Overview
The Bayflex (Model/Catalog Number: BASP 1010) is a medical device manufactured by EUCARE PHARMACEUTICALS PRIVATE LIMITED. This product is indexed under FDA Product Code / Category Classification M040503 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BASP 1010
- Product Code / EMDN
- M040503
- Device Name
- Bayflex
- Database Sync Date
- 2026-08-09 16:29:23
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 Bayflex?
The registered manufacturer of record for Bayflex is EUCARE PHARMACEUTICALS PRIVATE LIMITED.
What is the Primary UDI-DI identifier for Bayflex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08904085093631.
What classification code is assigned to this device?
This device is registered under product classification code M040503.
Similar Classification Devices (M040503)
Other Devices by EUCARE PHARMACEUTICALS PRIVATE LIMITED
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint