HOKAPI™ FT3 (UDI 06939716404748)
Manufactured by Suzhou Hokapi Biomedical Engineering Co., Ltd..
Device Regulatory Overview
The HOKAPI™ FT3 (Model/Catalog Number: 010301601) is a medical device manufactured by Suzhou Hokapi Biomedical Engineering Co., Ltd... This product is indexed under FDA Product Code / Category Classification W01020401 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 010301601
- Product Code / EMDN
- W01020401
- Device Name
- HOKAPI™ FT3
- Database Sync Date
- 2026-08-09 16:46:08
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 HOKAPI™ FT3?
The registered manufacturer of record for HOKAPI™ FT3 is Suzhou Hokapi Biomedical Engineering Co., Ltd...
What is the Primary UDI-DI identifier for HOKAPI™ FT3?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06939716404748.
What classification code is assigned to this device?
This device is registered under product classification code W01020401.
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Other Devices by Suzhou Hokapi Biomedical Engineering Co., Ltd..
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