eudamed_udi
Primary ID: 00076490794347
MEDI-GRIP Latex PF (UDI 00076490794347)
Manufactured by Ansell Healthcare Europe NV
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MEDI-GRIP Latex PF - Primary ID 00076490794347
Device Regulatory Overview
The MEDI-GRIP Latex PF (Model/Catalog Number: 330200690 Size 9.0) is a medical device manufactured by Ansell Healthcare Europe NV. This product is indexed under FDA Product Code / Category Classification T01010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 330200690 Size 9.0
- Product Code / EMDN
- T01010102
- Device Name
- Non-Powdered Latex Surgical Gloves
- Database Sync Date
- 2026-08-09 16:30:00
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 MEDI-GRIP Latex PF?
The registered manufacturer of record for MEDI-GRIP Latex PF is Ansell Healthcare Europe NV.
What is the Primary UDI-DI identifier for MEDI-GRIP Latex PF?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00076490794347.
What classification code is assigned to this device?
This device is registered under product classification code T01010102.
Similar Classification Devices (T01010102)
Other Devices by Ansell Healthcare Europe NV
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