MYCO WELL D-ONE SIX (UDI D-MS01379QA)
Manufactured by C.P.M. COMPAGNIA PER LA MEDICINA S.R.L.
Device Regulatory Overview
The MYCO WELL D-ONE SIX (Model/Catalog Number: MS01379) is a medical device manufactured by C.P.M. COMPAGNIA PER LA MEDICINA S.R.L.. This product is indexed under FDA Product Code / Category Classification W0104080207 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MS01379
- Product Code / EMDN
- W0104080207
- Device Name
- MYCO WELL D-ONE SIX
- Database Sync Date
- 2026-08-09 18:37:47
Full Regulatory Attributes
π 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 MYCO WELL D-ONE SIX?
The registered manufacturer of record for MYCO WELL D-ONE SIX is C.P.M. COMPAGNIA PER LA MEDICINA S.R.L..
What is the Primary UDI-DI identifier for MYCO WELL D-ONE SIX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-MS01379QA.
What classification code is assigned to this device?
This device is registered under product classification code W0104080207.
Similar Classification Devices (W0104080207)
Other Devices by C.P.M. COMPAGNIA PER LA MEDICINA S.R.L.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint