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.

Spéculum auriculaire à usage unique — 82 UDI-DI variants, MDR

MD Atlas
COMED SAS

Data from EUDAMED, last updated May 19, 2026

Spéculum auriculaire à usage unique

37011267247XXXXTS

82 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: COMED SAS

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: 37011267247XXXXTS
Device name: Spéculum auriculaire à usage unique
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 5, 2021

Manufacturer & authorised representative

Manufacturer

Name: COMED SAS
SRN: FR-MF-000000151
Country: France
Email: commercial@comed.fr
Phone: +33 3 88 77 13 00

Variants by status

UDI-DI variants

82 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

basicUdiUlid01FH7RDK9PVPYJFT9KZGMBDP8B

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

2470040BSD03701126704762
2470040BCBD03701126704625
2470040AHAL03701126704489
2471025AGI03701126705158
2470040BCJD03701126704656
2470125BGI03701126705059
2470025BCBD03701126704038

1 2 3 4