eudamed_udi
Primary ID: 08437027247231
DYNO RECHI (UDI 08437027247231)
Manufactured by Dyno Rechi
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DYNO RECHI - Primary ID 08437027247231
Device Regulatory Overview
The DYNO RECHI (Model/Catalog Number: 0116001S06) is a medical device manufactured by Dyno Rechi. This product is indexed under FDA Product Code / Category Classification Y060499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0116001S06
- Product Code / EMDN
- Y060499
- Device Name
- FAFA 3 BANDAS BLANCA T/S
- Database Sync Date
- 2026-08-09 18:08:32
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of DYNO RECHI?
The registered manufacturer of record for DYNO RECHI is Dyno Rechi.
What is the Primary UDI-DI identifier for DYNO RECHI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08437027247231.
What classification code is assigned to this device?
This device is registered under product classification code Y060499.
Similar Classification Devices (Y060499)
Other Devices by Dyno Rechi
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