eudamed_udi
Primary ID: 07333376013507
Nima 600 Tät Mesh 55x55 cm (UDI 07333376013507)
Manufactured by Nimacare AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Nima 600 Tät Mesh 55x55 cm - Primary ID 07333376013507
Device Regulatory Overview
The Nima 600 Tät Mesh 55x55 cm (Model/Catalog Number: 600TM5555) is a medical device manufactured by Nimacare AB. This product is indexed under FDA Product Code / Category Classification V08030102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 600TM5555
- Product Code / EMDN
- V08030102
- Device Name
- Nima 600 Tät Mesh
- Database Sync Date
- 2026-08-09 16:29:03
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 Nima 600 Tät Mesh 55x55 cm?
The registered manufacturer of record for Nima 600 Tät Mesh 55x55 cm is Nimacare AB.
What is the Primary UDI-DI identifier for Nima 600 Tät Mesh 55x55 cm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07333376013507.
What classification code is assigned to this device?
This device is registered under product classification code V08030102.
Similar Classification Devices (V08030102)
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