gudid
Primary ID: PE30
Canister (UDI PE30)
Manufactured by Shijiazhuang Yuanding Medical Device Co., LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Canister - Primary ID PE30
Device Regulatory Overview
The Canister (Model/Catalog Number: PE30) is a medical device manufactured by Shijiazhuang Yuanding Medical Device Co., LTD. This product is indexed under FDA Product Code / Category Classification KDQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PE30
- Product Code / EMDN
- KDQ
- Device Name
- Database Sync Date
- 2026-08-09 09:06:45
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 Canister?
The registered manufacturer of record for Canister is Shijiazhuang Yuanding Medical Device Co., LTD.
What is the Primary UDI-DI identifier for Canister?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PE30.
What classification code is assigned to this device?
This device is registered under product classification code KDQ.
Similar Classification Devices (KDQ)
Other Devices by Shijiazhuang Yuanding Medical Device Co., LTD
Programmatic Export
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