eudamed_udi
Primary ID: D-72900184696062W
GYNI ™ Scanner (UDI D-72900184696062W)
Manufactured by GynTools LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GYNI ™ Scanner - Primary ID D-72900184696062W
Device Regulatory Overview
The GYNI ™ Scanner (Model/Catalog Number: GTDS0000) is a medical device manufactured by GynTools LTD. This product is indexed under FDA Product Code / Category Classification W02029099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GTDS0000
- Product Code / EMDN
- W02029099
- Device Name
- GYNI ™ Scanner
- Database Sync Date
- 2026-08-09 17:18:52
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 GYNI ™ Scanner?
The registered manufacturer of record for GYNI ™ Scanner is GynTools LTD.
What is the Primary UDI-DI identifier for GYNI ™ Scanner?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-72900184696062W.
What classification code is assigned to this device?
This device is registered under product classification code W02029099.
Similar Classification Devices (W02029099)
Other Devices by GynTools LTD
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