gudid
Primary ID: 90111050
ClearPetra (UDI 90111050)
Manufactured by Well Lead Medical Co.,Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ClearPetra - Primary ID 90111050
Device Regulatory Overview
The ClearPetra (Model/Catalog Number: 90111050) is a medical device manufactured by Well Lead Medical Co.,Ltd. This product is indexed under FDA Product Code / Category Classification FED within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 90111050
- Product Code / EMDN
- FED
- Device Name
- ClearPetra Ureteral Access Sheath 10Fr x 50cm
- Database Sync Date
- 2026-08-09 09:04:58
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 ClearPetra?
The registered manufacturer of record for ClearPetra is Well Lead Medical Co.,Ltd.
What is the Primary UDI-DI identifier for ClearPetra?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 90111050.
What classification code is assigned to this device?
This device is registered under product classification code FED.
Similar Classification Devices (FED)
Other Devices by Well Lead Medical Co.,Ltd
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