Inorganic Phosphorous (IP) Test Kit (Phosphomolybdate) (UDI 06971674865155)
Manufactured by Biobase Biodustry(Shandong) Co.,Ltd.
Device Regulatory Overview
The Inorganic Phosphorous (IP) Test Kit (Phosphomolybdate) (Model/Catalog Number: R:40mL×4（716）) is a medical device manufactured by Biobase Biodustry(Shandong) Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W01010307 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- R:40mL×4（716）
- Product Code / EMDN
- W01010307
- Device Name
- Inorganic Phosphorous (IP) Test Kit (Phosphomolybdate)
- 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 Inorganic Phosphorous (IP) Test Kit (Phosphomolybdate)?
The registered manufacturer of record for Inorganic Phosphorous (IP) Test Kit (Phosphomolybdate) is Biobase Biodustry(Shandong) Co.,Ltd..
What is the Primary UDI-DI identifier for Inorganic Phosphorous (IP) Test Kit (Phosphomolybdate)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06971674865155.
What classification code is assigned to this device?
This device is registered under product classification code W01010307.
Similar Classification Devices (W01010307)
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