eudamed_udi
Primary ID: 56001726783320
Gripwise (UDI 56001726783320)
Manufactured by Gripwise Tech, Lda.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Gripwise - Primary ID 56001726783320
Device Regulatory Overview
The Gripwise (Model/Catalog Number: GW02) is a medical device manufactured by Gripwise Tech, Lda.. This product is indexed under FDA Product Code / Category Classification Y242103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GW02
- Product Code / EMDN
- Y242103
- Device Name
- Gripwise
- Database Sync Date
- 2026-08-09 17:22:48
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 Gripwise?
The registered manufacturer of record for Gripwise is Gripwise Tech, Lda..
What is the Primary UDI-DI identifier for Gripwise?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 56001726783320.
What classification code is assigned to this device?
This device is registered under product classification code Y242103.
Similar Classification Devices (Y242103)
Other Devices by Gripwise Tech, Lda.
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