eudamed_udi
Primary ID: 00806363505448
Naturflex (UDI 00806363505448)
Manufactured by Kanam Latex Industries Private Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Naturflex - Primary ID 00806363505448
Device Regulatory Overview
The Naturflex (Model/Catalog Number: 128918) is a medical device manufactured by Kanam Latex Industries Private Limited. This product is indexed under FDA Product Code / Category Classification T010201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 128918
- Product Code / EMDN
- T010201
- Device Name
- Sterile Latex Medical Examination Gloves Powdered
- Database Sync Date
- 2026-08-09 16:29:00
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 Naturflex?
The registered manufacturer of record for Naturflex is Kanam Latex Industries Private Limited.
What is the Primary UDI-DI identifier for Naturflex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00806363505448.
What classification code is assigned to this device?
This device is registered under product classification code T010201.
Similar Classification Devices (T010201)
Other Devices by Kanam Latex Industries Private Limited
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