eudamed_udi
Primary ID: 08028718200521
GINOCCHIERA ELASTICA REGOLABILE TAGLIA S (UDI 08028718200521)
Manufactured by PAVIS SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GINOCCHIERA ELASTICA REGOLABILE TAGLIA S - Primary ID 08028718200521
Device Regulatory Overview
The GINOCCHIERA ELASTICA REGOLABILE TAGLIA S (Model/Catalog Number: 020 BL S (BABY)) is a medical device manufactured by PAVIS SPA. This product is indexed under FDA Product Code / Category Classification Y061209 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 020 BL S (BABY)
- Product Code / EMDN
- Y061209
- Device Name
- LINEA GAMBA GINOCCHIO
- Database Sync Date
- 2026-08-09 16:45:05
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 GINOCCHIERA ELASTICA REGOLABILE TAGLIA S?
The registered manufacturer of record for GINOCCHIERA ELASTICA REGOLABILE TAGLIA S is PAVIS SPA.
What is the Primary UDI-DI identifier for GINOCCHIERA ELASTICA REGOLABILE TAGLIA S?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08028718200521.
What classification code is assigned to this device?
This device is registered under product classification code Y061209.
Similar Classification Devices (Y061209)
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