eudamed_udi
Primary ID: 06970614965160
Autoclave (UDI 06970614965160)
Manufactured by Shinva Medical Instrument Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Autoclave - Primary ID 06970614965160
Device Regulatory Overview
The Autoclave (Model/Catalog Number: Dmax-N) is a medical device manufactured by Shinva Medical Instrument Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z12011305 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Dmax-N
- Product Code / EMDN
- Z12011305
- Device Name
- Autoclave
- Database Sync Date
- 2026-08-09 16:29:58
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 Autoclave?
The registered manufacturer of record for Autoclave is Shinva Medical Instrument Co., Ltd..
What is the Primary UDI-DI identifier for Autoclave?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06970614965160.
What classification code is assigned to this device?
This device is registered under product classification code Z12011305.
Similar Classification Devices (Z12011305)
Other Devices by Shinva Medical Instrument Co., Ltd.
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