KIMTECH STERLING NITRILE EXAM GLOVES (L) (UDI 50708)
Manufactured by KIMBERLY-CLARK GLOBAL SALES, LLC
Device Regulatory Overview
The KIMTECH STERLING NITRILE EXAM GLOVES (L) (Model/Catalog Number: 50708) is a medical device manufactured by KIMBERLY-CLARK GLOBAL SALES, LLC. This product is indexed under FDA Product Code / Category Classification LZC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 50708
- Product Code / EMDN
- LZC
- Device Name
- Examination Gloves
- Database Sync Date
- 2026-08-09 09:08:52
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 KIMTECH STERLING NITRILE EXAM GLOVES (L)?
The registered manufacturer of record for KIMTECH STERLING NITRILE EXAM GLOVES (L) is KIMBERLY-CLARK GLOBAL SALES, LLC.
What is the Primary UDI-DI identifier for KIMTECH STERLING NITRILE EXAM GLOVES (L)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 50708.
What classification code is assigned to this device?
This device is registered under product classification code LZC.
Similar Classification Devices (LZC)
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