GUDIDData
eudamed_udi Primary ID: 08033481793392

Henke-ject Eco (UDI 08033481793392)

Manufactured by I.M.I. SNC DI MAZZUCATO PAOLO,ENRICO & C.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Henke-ject Eco - Primary ID 08033481793392

Device Regulatory Overview

The Henke-ject Eco (Model/Catalog Number: TC98N) 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 A02010203 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
TC98N
Product Code / EMDN
A02010203
Device Name
Single use Syringe 100/120ml
Database Sync Date
2026-08-09 17:01:15

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Henke-ject Eco?

The registered manufacturer of record for Henke-ject Eco is I.M.I. SNC DI MAZZUCATO PAOLO,ENRICO & C..

What is the Primary UDI-DI identifier for Henke-ject Eco?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08033481793392.

What classification code is assigned to this device?

This device is registered under product classification code A02010203.

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