Watin Biolife (UDI 06287044950308)
Manufactured by Watin Biolife Manufacturing Company
Device Regulatory Overview
The Watin Biolife (Model/Catalog Number: 1131) is a medical device manufactured by Watin Biolife Manufacturing Company. This product is indexed under FDA Product Code / Category Classification W0104010206 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1131
- Product Code / EMDN
- W0104010206
- Device Name
- MIDDLEBROOK 7H11 SELECTIVE AGAR SLANT
- Database Sync Date
- 2026-08-09 16:29:36
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 06287044950308.
What classification code is assigned to this device?
This device is registered under product classification code W0104010206.
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Other Devices by Watin Biolife Manufacturing Company
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