eudamed_udi
Primary ID: 07340047357594
BIMA (UDI 07340047357594)
Manufactured by B.I.M.A. PLASTTEKNIK AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BIMA - Primary ID 07340047357594
Device Regulatory Overview
The BIMA (Model/Catalog Number: B203-2) is a medical device manufactured by B.I.M.A. PLASTTEKNIK AB. This product is indexed under FDA Product Code / Category Classification V080399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- B203-2
- Product Code / EMDN
- V080399
- Device Name
- 73400473SITTCOXVA
- Database Sync Date
- 2026-08-09 16:28:55
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 BIMA?
The registered manufacturer of record for BIMA is B.I.M.A. PLASTTEKNIK AB.
What is the Primary UDI-DI identifier for BIMA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07340047357594.
What classification code is assigned to this device?
This device is registered under product classification code V080399.
Similar Classification Devices (V080399)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint