eudamed_udi
Primary ID: 08437027247439
FAJA REFUERZOS NEOPRENOT/M (UDI 08437027247439)
Manufactured by Dyno Rechi
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FAJA REFUERZOS NEOPRENOT/M - Primary ID 08437027247439
Device Regulatory Overview
The FAJA REFUERZOS NEOPRENOT/M (Model/Catalog Number: 0521502M07) is a medical device manufactured by Dyno Rechi. This product is indexed under FDA Product Code / Category Classification Y060307 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0521502M07
- Product Code / EMDN
- Y060307
- Device Name
- FAJA REFUERZOS NEOPRENO
- Database Sync Date
- 2026-08-09 16:28:51
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 FAJA REFUERZOS NEOPRENOT/M?
The registered manufacturer of record for FAJA REFUERZOS NEOPRENOT/M is Dyno Rechi.
What is the Primary UDI-DI identifier for FAJA REFUERZOS NEOPRENOT/M?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08437027247439.
What classification code is assigned to this device?
This device is registered under product classification code Y060307.
Similar Classification Devices (Y060307)
Other Devices by Dyno Rechi
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint