gudid
Primary ID: 36-ML3535 MK8-STK
Vyaire (UDI 36-ML3535 MK8-STK)
Manufactured by Jaeger Medical GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vyaire - Primary ID 36-ML3535 MK8-STK
Device Regulatory Overview
The Vyaire (Model/Catalog Number: 36-ML3535 MK8-STK) is a medical device manufactured by Jaeger Medical GmbH. This product is indexed under FDA Product Code / Category Classification BZG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 36-ML3535 MK8-STK
- Product Code / EMDN
- BZG
- Device Name
- MicroLoop
- Database Sync Date
- 2026-08-09 09:16:52
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 Vyaire?
The registered manufacturer of record for Vyaire is Jaeger Medical GmbH.
What is the Primary UDI-DI identifier for Vyaire?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 36-ML3535 MK8-STK.
What classification code is assigned to this device?
This device is registered under product classification code BZG.
Similar Classification Devices (BZG)
Other Devices by Jaeger Medical GmbH
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