INDICAID™ Mycoplasma Pneumoniae (MP) Rapid IgM Antibody Test (UDI D-A017CY)
Manufactured by Phase Scientific International Limited
Device Regulatory Overview
The INDICAID™ Mycoplasma Pneumoniae (MP) Rapid IgM Antibody Test (Model/Catalog Number: INDICAID™ Mycoplasma Pneumoniae (MP) Rapid IgM Antibody Test) is a medical device manufactured by Phase Scientific International Limited. This product is indexed under FDA Product Code / Category Classification W0105090199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- INDICAID™ Mycoplasma Pneumoniae (MP) Rapid IgM Antibody Test
- Product Code / EMDN
- W0105090199
- Device Name
- INDICAID™ Mycoplasma Pneumoniae (MP) Rapid IgM Antibody Test
- Database Sync Date
- 2026-08-09 16:51:47
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 INDICAID™ Mycoplasma Pneumoniae (MP) Rapid IgM Antibody Test?
The registered manufacturer of record for INDICAID™ Mycoplasma Pneumoniae (MP) Rapid IgM Antibody Test is Phase Scientific International Limited.
What is the Primary UDI-DI identifier for INDICAID™ Mycoplasma Pneumoniae (MP) Rapid IgM Antibody Test?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-A017CY.
What classification code is assigned to this device?
This device is registered under product classification code W0105090199.
Similar Classification Devices (W0105090199)
Other Devices by Phase Scientific International Limited
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