CONTENITORE PP TAPPO PRESSIONE SERIGRAFATO 250 ml (UDI 08055510560010)
Manufactured by Kaltek S.r.l.
Device Regulatory Overview
The CONTENITORE PP TAPPO PRESSIONE SERIGRAFATO 250 ml (Model/Catalog Number: 0101) is a medical device manufactured by Kaltek S.r.l.. This product is indexed under FDA Product Code / Category Classification W050301029099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0101
- Product Code / EMDN
- W050301029099
- Device Name
- CONTENITORI PER CAMPIONI ISTOLOGICI
- Database Sync Date
- 2026-08-09 16:30:37
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 CONTENITORE PP TAPPO PRESSIONE SERIGRAFATO 250 ml?
The registered manufacturer of record for CONTENITORE PP TAPPO PRESSIONE SERIGRAFATO 250 ml is Kaltek S.r.l..
What is the Primary UDI-DI identifier for CONTENITORE PP TAPPO PRESSIONE SERIGRAFATO 250 ml?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08055510560010.
What classification code is assigned to this device?
This device is registered under product classification code W050301029099.
Similar Classification Devices (W050301029099)
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