eudamed_udi
Primary ID: 08028718478111
CORSETTO ORTHO-E (H.21) CREMA M (UDI 08028718478111)
Manufactured by PAVIS SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CORSETTO ORTHO-E (H.21) CREMA M - Primary ID 08028718478111
Device Regulatory Overview
The CORSETTO ORTHO-E (H.21) CREMA M (Model/Catalog Number: 553 H21 CR M) is a medical device manufactured by PAVIS SPA. This product is indexed under FDA Product Code / Category Classification Y060308 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 553 H21 CR M
- Product Code / EMDN
- Y060308
- Device Name
- LINEA SCHIENA
- Database Sync Date
- 2026-08-09 16:46:08
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 CORSETTO ORTHO-E (H.21) CREMA M?
The registered manufacturer of record for CORSETTO ORTHO-E (H.21) CREMA M is PAVIS SPA.
What is the Primary UDI-DI identifier for CORSETTO ORTHO-E (H.21) CREMA M?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08028718478111.
What classification code is assigned to this device?
This device is registered under product classification code Y060308.
Similar Classification Devices (Y060308)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint