eudamed_udi
Primary ID: 05600961537659
SteriKit (UDI 05600961537659)
Manufactured by Fapomed- Dispositivos Médicos, S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SteriKit - Primary ID 05600961537659
Device Regulatory Overview
The SteriKit (Model/Catalog Number: AC.160010) is a medical device manufactured by Fapomed- Dispositivos Médicos, S.A.. This product is indexed under FDA Product Code / Category Classification T020102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AC.160010
- Product Code / EMDN
- T020102
- Device Name
- Epidural drape with aperture, 15x10 cm
- Database Sync Date
- 2026-08-09 16:29:26
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 SteriKit?
The registered manufacturer of record for SteriKit is Fapomed- Dispositivos Médicos, S.A..
What is the Primary UDI-DI identifier for SteriKit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05600961537659.
What classification code is assigned to this device?
This device is registered under product classification code T020102.
Similar Classification Devices (T020102)
Other Devices by Fapomed- Dispositivos Médicos, S.A.
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