Superflex (UDI 00806363505370)
Manufactured by Kanam Latex Industries Private Limited
Device Regulatory Overview
The Superflex (Model/Catalog Number: 148061) is a medical device manufactured by Kanam Latex Industries Private Limited. This product is indexed under FDA Product Code / Category Classification T01010203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 148061
- Product Code / EMDN
- T01010203
- Device Name
- Sterile Synthetic Surgical Gloves Powder Free – Poly Isoprene
- Database Sync Date
- 2026-08-09 16:28:57
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 Superflex?
The registered manufacturer of record for Superflex is Kanam Latex Industries Private Limited.
What is the Primary UDI-DI identifier for Superflex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00806363505370.
What classification code is assigned to this device?
This device is registered under product classification code T01010203.
Similar Classification Devices (T01010203)
Other Devices by Kanam Latex Industries Private Limited
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