eudamed_udi
Primary ID: D-ZVT0123B6
Spacer (UDI D-ZVT0123B6)
Manufactured by Cipla Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Spacer - Primary ID D-ZVT0123B6
Device Regulatory Overview
The Spacer (Model/Catalog Number: NA) is a medical device manufactured by Cipla Limited. This product is indexed under FDA Product Code / Category Classification R9001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NA
- Product Code / EMDN
- R9001
- Device Name
- Spacer
- Database Sync Date
- 2026-08-09 17:35:44
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 Spacer?
The registered manufacturer of record for Spacer is Cipla Limited.
What is the Primary UDI-DI identifier for Spacer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-ZVT0123B6.
What classification code is assigned to this device?
This device is registered under product classification code R9001.
Similar Classification Devices (R9001)
Other Devices by Cipla Limited
Programmatic Export
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JSON API Endpoint