eudamed_udi
Primary ID: 06975181140040
Multichamber™ (UDI 06975181140040)
Manufactured by Hopfly Biotech (Huzhou) CO., LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Multichamber™ - Primary ID 06975181140040
Device Regulatory Overview
The Multichamber™ (Model/Catalog Number: Multichamber™) is a medical device manufactured by Hopfly Biotech (Huzhou) CO., LTD. This product is indexed under FDA Product Code / Category Classification A1102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Multichamber™
- Product Code / EMDN
- A1102
- Device Name
- Viral Transport Medium
- Database Sync Date
- 2026-08-09 16:28:46
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 Multichamber™?
The registered manufacturer of record for Multichamber™ is Hopfly Biotech (Huzhou) CO., LTD.
What is the Primary UDI-DI identifier for Multichamber™?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975181140040.
What classification code is assigned to this device?
This device is registered under product classification code A1102.
Similar Classification Devices (A1102)
Other Devices by Hopfly Biotech (Huzhou) CO., LTD
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint