eudamed_udi
Primary ID: 08028718478739
CORSETTO ORTHO-E (H.21) GRIGIO SCURO XL (UDI 08028718478739)
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) GRIGIO SCURO XL - Primary ID 08028718478739
Device Regulatory Overview
The CORSETTO ORTHO-E (H.21) GRIGIO SCURO XL (Model/Catalog Number: 553 H21 GS XL) 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 GS XL
- Product Code / EMDN
- Y060308
- Device Name
- LINEA SCHIENA
- Database Sync Date
- 2026-08-09 16:51:37
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 CORSETTO ORTHO-E (H.21) GRIGIO SCURO XL?
The registered manufacturer of record for CORSETTO ORTHO-E (H.21) GRIGIO SCURO XL is PAVIS SPA.
What is the Primary UDI-DI identifier for CORSETTO ORTHO-E (H.21) GRIGIO SCURO XL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08028718478739.
What classification code is assigned to this device?
This device is registered under product classification code Y060308.
Similar Classification Devices (Y060308)
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