eudamed_udi
Primary ID: 08905159001811
NULIFE (UDI 08905159001811)
Manufactured by MRK HEALTHCARE PVT. LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NULIFE - Primary ID 08905159001811
Device Regulatory Overview
The NULIFE (Model/Catalog Number: SRGLUE) is a medical device manufactured by MRK HEALTHCARE PVT. LTD.. This product is indexed under FDA Product Code / Category Classification T01010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SRGLUE
- Product Code / EMDN
- T01010102
- Device Name
- Latex Surgical Gloves, Powder Free
- Database Sync Date
- 2026-08-09 16:28:48
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 NULIFE?
The registered manufacturer of record for NULIFE is MRK HEALTHCARE PVT. LTD..
What is the Primary UDI-DI identifier for NULIFE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08905159001811.
What classification code is assigned to this device?
This device is registered under product classification code T01010102.
Similar Classification Devices (T01010102)
Other Devices by MRK HEALTHCARE PVT. LTD.
Programmatic Export
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