eudamed_udi
Primary ID: 10704411018834
AMSure® SUTURE REMOVAL KIT (UDI 10704411018834)
Manufactured by Amsino International Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AMSure® SUTURE REMOVAL KIT - Primary ID 10704411018834
Device Regulatory Overview
The AMSure® SUTURE REMOVAL KIT (Model/Catalog Number: SRT001) is a medical device manufactured by Amsino International Inc.. This product is indexed under FDA Product Code / Category Classification Q030305 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SRT001
- Product Code / EMDN
- Q030305
- Device Name
- Suture Removal Kit
- Database Sync Date
- 2026-08-09 17:06:32
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 AMSure® SUTURE REMOVAL KIT?
The registered manufacturer of record for AMSure® SUTURE REMOVAL KIT is Amsino International Inc..
What is the Primary UDI-DI identifier for AMSure® SUTURE REMOVAL KIT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10704411018834.
What classification code is assigned to this device?
This device is registered under product classification code Q030305.
Similar Classification Devices (Q030305)
Other Devices by Amsino International Inc.
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