Cannula preleva latte 20 cm GD, per uso enterale- NUTRIFIT (UDI 08015262037413)
Manufactured by PENTAFERTE ITALIA SRL
Device Regulatory Overview
The Cannula preleva latte 20 cm GD, per uso enterale- NUTRIFIT (Model/Catalog Number: 817.208) is a medical device manufactured by PENTAFERTE ITALIA SRL. This product is indexed under FDA Product Code / Category Classification A020108 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 817.208
- Product Code / EMDN
- A020108
- Device Name
- SIRINGHE E ACCESSORI ENTERALI
- Database Sync Date
- 2026-08-09 16:46:47
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 Cannula preleva latte 20 cm GD, per uso enterale- NUTRIFIT?
The registered manufacturer of record for Cannula preleva latte 20 cm GD, per uso enterale- NUTRIFIT is PENTAFERTE ITALIA SRL.
What is the Primary UDI-DI identifier for Cannula preleva latte 20 cm GD, per uso enterale- NUTRIFIT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08015262037413.
What classification code is assigned to this device?
This device is registered under product classification code A020108.
Similar Classification Devices (A020108)
Other Devices by PENTAFERTE ITALIA SRL
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