eudamed_udi
Primary ID: 03615800052677
QUIEGO 1000 v2 (GRIS BEIGE 1019/PRUNE) (UDI 03615800052677)
Manufactured by VILGO
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for QUIEGO 1000 v2 (GRIS BEIGE 1019/PRUNE) - Primary ID 03615800052677
Device Regulatory Overview
The QUIEGO 1000 v2 (GRIS BEIGE 1019/PRUNE) (Model/Catalog Number: 2070096S27) is a medical device manufactured by VILGO. This product is indexed under FDA Product Code / Category Classification V080202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2070096S27
- Product Code / EMDN
- V080202
- Device Name
- QUIEGO 1000
- Database Sync Date
- 2026-08-09 16:30:22
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 QUIEGO 1000 v2 (GRIS BEIGE 1019/PRUNE)?
The registered manufacturer of record for QUIEGO 1000 v2 (GRIS BEIGE 1019/PRUNE) is VILGO.
What is the Primary UDI-DI identifier for QUIEGO 1000 v2 (GRIS BEIGE 1019/PRUNE)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03615800052677.
What classification code is assigned to this device?
This device is registered under product classification code V080202.
Similar Classification Devices (V080202)
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