eudamed_udi
Primary ID: 08944000597219
JMI (UDI 08944000597219)
Manufactured by JMI SYRINGES & MEDICAL DEVICES LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for JMI - Primary ID 08944000597219
Device Regulatory Overview
The JMI (Model/Catalog Number: FP6016) is a medical device manufactured by JMI SYRINGES & MEDICAL DEVICES LTD.. This product is indexed under FDA Product Code / Category Classification A020102010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FP6016
- Product Code / EMDN
- A020102010101
- Device Name
- FP6016: Sterile, Single Use, Hypodermic Disposable Syringe (DS), 50ml Luer Slip with Hypodermic Needle 21G x 1¼” (0.80 mm x 32 mm)
- Database Sync Date
- 2026-08-09 16:50:19
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 JMI?
The registered manufacturer of record for JMI is JMI SYRINGES & MEDICAL DEVICES LTD..
What is the Primary UDI-DI identifier for JMI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08944000597219.
What classification code is assigned to this device?
This device is registered under product classification code A020102010101.
Similar Classification Devices (A020102010101)
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