Transflux CT 250 (UDI 05600988820598)
Manufactured by BHL-Medical, Indústria de Produtos Hospitalares, lda
Device Regulatory Overview
The Transflux CT 250 (Model/Catalog Number: PR-20203) is a medical device manufactured by BHL-Medical, Indústria de Produtos Hospitalares, lda. This product is indexed under FDA Product Code / Category Classification A03020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PR-20203
- Product Code / EMDN
- A03020101
- Device Name
- Transflux
- Database Sync Date
- 2026-08-09 16:29:07
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 Transflux CT 250?
The registered manufacturer of record for Transflux CT 250 is BHL-Medical, Indústria de Produtos Hospitalares, lda.
What is the Primary UDI-DI identifier for Transflux CT 250?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05600988820598.
What classification code is assigned to this device?
This device is registered under product classification code A03020101.
Similar Classification Devices (A03020101)
Other Devices by BHL-Medical, Indústria de Produtos Hospitalares, lda
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint