sempermed syntegra preCision (UDI 09001570557858)
Manufactured by HARPS Investment Asia Pte. Ltd.
Device Regulatory Overview
The sempermed syntegra preCision (Model/Catalog Number: 3000016674) is a medical device manufactured by HARPS Investment Asia Pte. Ltd.. This product is indexed under FDA Product Code / Category Classification T01010203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3000016674
- Product Code / EMDN
- T01010203
- Device Name
- Sterile, single use, powder free, synthetic polyisoprene, surgical glove, anatomically shaped, cream
- Database Sync Date
- 2026-08-09 16:50:18
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 sempermed syntegra preCision?
The registered manufacturer of record for sempermed syntegra preCision is HARPS Investment Asia Pte. Ltd..
What is the Primary UDI-DI identifier for sempermed syntegra preCision?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09001570557858.
What classification code is assigned to this device?
This device is registered under product classification code T01010203.
Similar Classification Devices (T01010203)
Other Devices by HARPS Investment Asia Pte. Ltd.
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