IMI (UDI 08033481791718)
Manufactured by I.M.I. SNC DI MAZZUCATO PAOLO,ENRICO & C.
Device Regulatory Overview
The IMI (Model/Catalog Number: TE99N) is a medical device manufactured by I.M.I. SNC DI MAZZUCATO PAOLO,ENRICO & C.. This product is indexed under FDA Product Code / Category Classification A020102010202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TE99N
- Product Code / EMDN
- A020102010202
- Device Name
- Single use syringe
- Database Sync Date
- 2026-08-09 16:48:01
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 IMI?
The registered manufacturer of record for IMI is I.M.I. SNC DI MAZZUCATO PAOLO,ENRICO & C..
What is the Primary UDI-DI identifier for IMI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08033481791718.
What classification code is assigned to this device?
This device is registered under product classification code A020102010202.
Similar Classification Devices (A020102010202)
Other Devices by I.M.I. SNC DI MAZZUCATO PAOLO,ENRICO & C.
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