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

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Countersink — 3 UDI-DI variants, MDR (DEEP Company)

MD Atlas
DEEP Company

Data from EUDAMED, last updated May 19, 2026

Countersink

3665588COUNT200EW

3 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: DEEP Company

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 3665588COUNT200EW
Device name: Countersink
Device model: DESIGN
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: DEEP Company
SRN: FR-MF-000009485
Country: France
Email: sguern@deep-company.com
Phone: +33 6 63 27 45 15

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KMMH646RWEDQ9KHGZ5XPSGZ0

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

Countersink - 4 mm diameter03665588007406
Countersink - 5 mm diameter03665588007413
Countersink - 6,5 mm diameter03665588007420