eudamed_udi
Primary ID: 09557795006287
PROFEEL DHD PI (UDI 09557795006287)
Manufactured by WRP Asia Pacific Sdn. Bhd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PROFEEL DHD PI - Primary ID 09557795006287
Device Regulatory Overview
The PROFEEL DHD PI (Model/Catalog Number: P3380-56) 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
- P3380-56
- Product Code / EMDN
- T01010203
- Device Name
- Polyisoprene Surgical Gloves, Powder Free, Sterile
- Database Sync Date
- 2026-08-09 16:59:21
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 DHD PI?
The registered manufacturer of record for PROFEEL DHD PI is WRP Asia Pacific Sdn. Bhd..
What is the Primary UDI-DI identifier for PROFEEL DHD PI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09557795006287.
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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