gudid
Primary ID: 1
AMSafe I.V. Administration Set (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 - Primary ID 1
Device Regulatory Overview
The AMSafe I.V. Administration Set (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 Set100" (254 cm) Long, Non-Pyrogenic fluid pathway. GRAVITY USE ONLY
- 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?
The registered manufacturer of record for AMSafe I.V. Administration Set is AMSINO INTERNATIONAL, INC..
What is the Primary UDI-DI identifier for AMSafe I.V. Administration Set?
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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