GUDIDData
eudamed_udi Primary ID: D-8901117ZVT0123369Q

Zerostat VT Spacer (UDI D-8901117ZVT0123369Q)

Manufactured by Cipla Limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Zerostat VT Spacer - Primary ID D-8901117ZVT0123369Q

Device Regulatory Overview

The Zerostat VT Spacer (Model/Catalog Number: Not Applicable for Zerostat VT Spacer) is a medical device manufactured by Cipla Limited. This product is indexed under FDA Product Code / Category Classification R9099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
Not Applicable for Zerostat VT Spacer
Product Code / EMDN
R9099
Device Name
Zerostat VT Spacer
Database Sync Date
2026-08-09 18:25:17

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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Frequently Asked Questions

Who is the primary manufacturer of Zerostat VT Spacer?

The registered manufacturer of record for Zerostat VT Spacer is Cipla Limited.

What is the Primary UDI-DI identifier for Zerostat VT Spacer?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-8901117ZVT0123369Q.

What classification code is assigned to this device?

This device is registered under product classification code R9099.

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