dermagel coated (UDI 00806363504427)
Manufactured by Kanam Latex Industries Private Limited
Device Regulatory Overview
The dermagel coated (Model/Catalog Number: RC10075060_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
- RC10075060_0016
- Product Code / EMDN
- T01010102
- Device Name
- Sterile Latex Surgical Gloves Powder Free
- Database Sync Date
- 2026-08-09 16:30:29
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 dermagel coated?
The registered manufacturer of record for dermagel coated is Kanam Latex Industries Private Limited.
What is the Primary UDI-DI identifier for dermagel coated?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00806363504427.
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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