Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Non-Powdered Latex Surgical Gloves — 8 UDI-DI variants, MDR

MD Atlas
Ansell Healthcare Europe NV

Data from EUDAMED, last updated May 23, 2026

Non-Powdered Latex Surgical Gloves

5414566MGLATPF3302006MD

8 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Ansell Healthcare Europe NV

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5414566MGLATPF3302006MD
Device name: Non-Powdered Latex Surgical Gloves
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Aug 11, 2025

Manufacturer & authorised representative

Manufacturer

Name: Ansell Healthcare Europe NV
SRN: BE-MF-000000691
Country: Belgium
Email: samantha.marshall@ansell.com
Phone: +447919410683

Variants by status

UDI-DI variants

8 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01K2CHWV344HC5S66AG4QGE69Y

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

330200660 Size 6.000076490794286
330200685 Size 8.500076490794330
330200690 Size 9.000076490794347
330200680 Size 8.000076490794323
330200675 Size 7.500076490794316
330200665 Size 6.500076490794293
330200655 Size 5.500076490794279
330200670 Size 7.000076490794309