eudamed_udi
Primary ID: 08430655900233
E74 KINESIOTAPE (UDI 08430655900233)
Manufactured by Calvo Izquierdo S.L.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for E74 KINESIOTAPE - Primary ID 08430655900233
Device Regulatory Overview
The E74 KINESIOTAPE (Model/Catalog Number: 12002-51) is a medical device manufactured by Calvo Izquierdo S.L.. This product is indexed under FDA Product Code / Category Classification M030299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 12002-51
- Product Code / EMDN
- M030299
- Device Name
- C+I KINESIOTAPE
- Database Sync Date
- 2026-08-09 17:13:22
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 E74 KINESIOTAPE?
The registered manufacturer of record for E74 KINESIOTAPE is Calvo Izquierdo S.L..
What is the Primary UDI-DI identifier for E74 KINESIOTAPE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08430655900233.
What classification code is assigned to this device?
This device is registered under product classification code M030299.
Similar Classification Devices (M030299)
Other Devices by Calvo Izquierdo S.L.
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