eudamed_udi
Primary ID: 06970150906511
Mycoplasma IES Plus (UDI 06970150906511)
Manufactured by Autobio Diagnostics Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Mycoplasma IES Plus - Primary ID 06970150906511
Device Regulatory Overview
The Mycoplasma IES Plus (Model/Catalog Number: MA06) is a medical device manufactured by Autobio Diagnostics Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0104080207 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MA06
- Product Code / EMDN
- W0104080207
- Device Name
- /
- Database Sync Date
- 2026-08-09 17:02:13
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 Mycoplasma IES Plus?
The registered manufacturer of record for Mycoplasma IES Plus is Autobio Diagnostics Co., Ltd..
What is the Primary UDI-DI identifier for Mycoplasma IES Plus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06970150906511.
What classification code is assigned to this device?
This device is registered under product classification code W0104080207.
Similar Classification Devices (W0104080207)
Other Devices by Autobio Diagnostics Co., Ltd.
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