PROFEEL DOUBLE GLOVING NON-LATEX (UDI 09557795011083)
Manufactured by WRP Asia Pacific Sdn. Bhd.
Device Regulatory Overview
The PROFEEL DOUBLE GLOVING NON-LATEX (Model/Catalog Number: P3360-62) is a medical device manufactured by WRP Asia Pacific Sdn. Bhd.. This product is indexed under FDA Product Code / Category Classification T01010203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- P3360-62
- Product Code / EMDN
- T01010203
- Device Name
- Polyisoprene Surgical Gloves, Powder Free, Sterile
- Database Sync Date
- 2026-08-09 17:01:24
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 PROFEEL DOUBLE GLOVING NON-LATEX?
The registered manufacturer of record for PROFEEL DOUBLE GLOVING NON-LATEX is WRP Asia Pacific Sdn. Bhd..
What is the Primary UDI-DI identifier for PROFEEL DOUBLE GLOVING NON-LATEX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09557795011083.
What classification code is assigned to this device?
This device is registered under product classification code T01010203.
Similar Classification Devices (T01010203)
Other Devices by WRP Asia Pacific Sdn. Bhd.
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