eudamed_udi
Primary ID: 09551012401275
Sempermed Syntegra X (UDI 09551012401275)
Manufactured by Ineo Tech Sdn Bhd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sempermed Syntegra X - Primary ID 09551012401275
Device Regulatory Overview
The Sempermed Syntegra X (Model/Catalog Number: 3000016276) is a medical device manufactured by Ineo Tech Sdn Bhd. This product is indexed under FDA Product Code / Category Classification T01010203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3000016276
- Product Code / EMDN
- T01010203
- Device Name
- Radiation Attenuating Surgical Gloves, Polyisoprene, Powder Free
- Database Sync Date
- 2026-08-09 16:28:51
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 X?
The registered manufacturer of record for Sempermed Syntegra X is Ineo Tech Sdn Bhd.
What is the Primary UDI-DI identifier for Sempermed Syntegra X?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09551012401275.
What classification code is assigned to this device?
This device is registered under product classification code T01010203.
Similar Classification Devices (T01010203)
Other Devices by Ineo Tech Sdn Bhd
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