eudamed_udi
Primary ID: 07640142190646
Spirette FA Pro/LAB (basic unit) (UDI 07640142190646)
Manufactured by NDD Medizintechnik AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Spirette FA Pro/LAB (basic unit) - Primary ID 07640142190646
Device Regulatory Overview
The Spirette FA Pro/LAB (basic unit) (Model/Catalog Number: 2050-70) is a medical device manufactured by NDD Medizintechnik AG. This product is indexed under FDA Product Code / Category Classification Z12150185 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2050-70
- Product Code / EMDN
- Z12150185
- Device Name
- Breathing tubes
- Database Sync Date
- 2026-08-09 17:38:46
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 Spirette FA Pro/LAB (basic unit)?
The registered manufacturer of record for Spirette FA Pro/LAB (basic unit) is NDD Medizintechnik AG.
What is the Primary UDI-DI identifier for Spirette FA Pro/LAB (basic unit)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07640142190646.
What classification code is assigned to this device?
This device is registered under product classification code Z12150185.
Similar Classification Devices (Z12150185)
Other Devices by NDD Medizintechnik AG
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