santex powder-free (UDI 00806363501341)
Manufactured by Kanam Latex Industries Private Limited
Device Regulatory Overview
The santex powder-free (Model/Catalog Number: RC10051075_0016) is a medical device manufactured by Kanam Latex Industries Private Limited. This product is indexed under FDA Product Code / Category Classification T01010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RC10051075_0016
- Product Code / EMDN
- T01010102
- Device Name
- Sterile Latex Surgical Gloves Powder Free
- Database Sync Date
- 2026-08-09 16:30:40
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 santex powder-free?
The registered manufacturer of record for santex powder-free is Kanam Latex Industries Private Limited.
What is the Primary UDI-DI identifier for santex powder-free?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00806363501341.
What classification code is assigned to this device?
This device is registered under product classification code T01010102.
Similar Classification Devices (T01010102)
Other Devices by Kanam Latex Industries Private Limited
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