gudid
Primary ID: 1
AMSafe I.V. Administration Set 106 (UDI 1)
Manufactured by AMSINO INTERNATIONAL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AMSafe I.V. Administration Set 106 - Primary ID 1
Device Regulatory Overview
The AMSafe I.V. Administration Set 106 (Model/Catalog Number: 1) is a medical device manufactured by AMSINO INTERNATIONAL, INC.. This product is indexed under FDA Product Code / Category Classification FPA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1
- Product Code / EMDN
- FPA
- Device Name
- AMSafe I.V. Administration Set 106For use with Spectrum, Flo-Gard 6201 and 6301 series pumps106 (2.6m), 10 drops/mL, Slide and Roller Clamp, Backcheck Valve,0.22 Micron Filter, (2) Sure-Lok Needle-Free valves,Rotating Male Luer Lock with Retractable Collar,Approx. Priming Volume: 22mL
- Database Sync Date
- 2026-08-09 10:01:11
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 AMSafe I.V. Administration Set 106?
The registered manufacturer of record for AMSafe I.V. Administration Set 106 is AMSINO INTERNATIONAL, INC..
What is the Primary UDI-DI identifier for AMSafe I.V. Administration Set 106?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.
What classification code is assigned to this device?
This device is registered under product classification code FPA.
Similar Classification Devices (FPA)
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