Unspecified Brand (UDI 05051223035428)
Manufactured by Unimicro Medical Systems (Shenzhen) Co., Ltd
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: PS1322) is a medical device manufactured by Unimicro Medical Systems (Shenzhen) Co., Ltd. This product is indexed under FDA Product Code / Category Classification K01010103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PS1322
- Product Code / EMDN
- K01010103
- Device Name
- Elite Optical Balloon Trocar 12mm x 100mm with Additional Cannula
- Database Sync Date
- 2026-08-09 16:28:56
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Unimicro Medical Systems (Shenzhen) Co., Ltd.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05051223035428.
What classification code is assigned to this device?
This device is registered under product classification code K01010103.
Similar Classification Devices (K01010103)
Other Devices by Unimicro Medical Systems (Shenzhen) Co., Ltd
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint