Saugrohr m.Unterbr. u. Mandrin ø 2,5 mm 17,5 cm (UDI 04250379887795)
Manufactured by Zepf Medical Instruments GmbH
Device Regulatory Overview
The Saugrohr m.Unterbr. u. Mandrin ø 2,5 mm 17,5 cm (Model/Catalog Number: 40-3301-17) is a medical device manufactured by Zepf Medical Instruments GmbH. This product is indexed under FDA Product Code / Category Classification L030101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 40-3301-17
- Product Code / EMDN
- L030101
- Device Name
- Kanüle, Absaugung
- Database Sync Date
- 2026-08-09 16:28:45
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 Saugrohr m.Unterbr. u. Mandrin ø 2,5 mm 17,5 cm?
The registered manufacturer of record for Saugrohr m.Unterbr. u. Mandrin ø 2,5 mm 17,5 cm is Zepf Medical Instruments GmbH.
What is the Primary UDI-DI identifier for Saugrohr m.Unterbr. u. Mandrin ø 2,5 mm 17,5 cm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250379887795.
What classification code is assigned to this device?
This device is registered under product classification code L030101.
Similar Classification Devices (L030101)
Other Devices by Zepf Medical Instruments GmbH
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