Watin Biolife (UDI 06287044950742)
Manufactured by Watin Biolife Manufacturing Company
Device Regulatory Overview
The Watin Biolife (Model/Catalog Number: 2090 - 6600) is a medical device manufactured by Watin Biolife Manufacturing Company. This product is indexed under FDA Product Code / Category Classification W0104010499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2090 - 6600
- Product Code / EMDN
- W0104010499
- Device Name
- HAEMOPHILUS TEST MEDIUM
- Database Sync Date
- 2026-08-09 16:29:20
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 Watin Biolife?
The registered manufacturer of record for Watin Biolife is Watin Biolife Manufacturing Company.
What is the Primary UDI-DI identifier for Watin Biolife?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06287044950742.
What classification code is assigned to this device?
This device is registered under product classification code W0104010499.
Similar Classification Devices (W0104010499)
Other Devices by Watin Biolife Manufacturing Company
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