gudid
Primary ID: U12A010110
Specimen Collection Bottle (UDI U12A010110)
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 Specimen Collection Bottle - Primary ID U12A010110
Device Regulatory Overview
The Specimen Collection Bottle (Model/Catalog Number: U12A010110) is a medical device manufactured by Well Lead Medical Co.,Ltd. This product is indexed under FDA Product Code / Category Classification FMH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- U12A010110
- Product Code / EMDN
- FMH
- Device Name
- 200ml
- 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 Specimen Collection Bottle?
The registered manufacturer of record for Specimen Collection Bottle is Well Lead Medical Co.,Ltd.
What is the Primary UDI-DI identifier for Specimen Collection Bottle?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is U12A010110.
What classification code is assigned to this device?
This device is registered under product classification code FMH.
Similar Classification Devices (FMH)
Other Devices by Well Lead Medical Co.,Ltd
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