eudamed_udi
Primary ID: 08906164420178
NEOLIFE (UDI 08906164420178)
Manufactured by AADHAR MEDICARE PRIVATE LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NEOLIFE - Primary ID 08906164420178
Device Regulatory Overview
The NEOLIFE (Model/Catalog Number: CS-05) is a medical device manufactured by AADHAR MEDICARE PRIVATE LIMITED. This product is indexed under FDA Product Code / Category Classification M030501 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CS-05
- Product Code / EMDN
- M030501
- Device Name
- Cervical Support
- Database Sync Date
- 2026-08-09 16:28:46
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 NEOLIFE?
The registered manufacturer of record for NEOLIFE is AADHAR MEDICARE PRIVATE LIMITED.
What is the Primary UDI-DI identifier for NEOLIFE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08906164420178.
What classification code is assigned to this device?
This device is registered under product classification code M030501.
Similar Classification Devices (M030501)
Other Devices by AADHAR MEDICARE PRIVATE LIMITED
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