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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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Organization name
UDI-DI code
Reference / catalog number

Countersink - 4 mm diameter — Class IIa MDR by DEEP Company

MD Atlas
DEEP Company

EUDAMED last updated this device on Mar 26, 2026

Countersink - 4 mm diameter

3665588COUNT200EW

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: DEEP Company
UDI-DI code: 03665588007406
Reference / catalog number: PFD30-I91044000

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Manufacturer information

Organization name: DEEP Company
SRN: FR-MF-000009485
Manufacturer status: Active

Related devices

Countersink - 5 mm diameter3665588COUNT200EWOn the market Countersink - 6,5 mm diameter3665588COUNT200EWOn the market Design I implant 3,5 diameter - 10 mm lenght3665588IMPLT201EROn the market Design I implant 3,5 diameter - 8 mm lenght3665588IMPLT201EROn the market Healing Abutment 4 diameter - 1 mm height3665588PCICA2003FOn the market

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Feb 27, 2026	Mar 26, 2026

Device identification

Trade name: Countersink - 4 mm diameter
UDI-DI code: 03665588007406
Basic UDI-DI: 3665588COUNT200EW
Reference / catalog number: PFD30-I91044000
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: https://astem.fr/documentation/
Clinical sizes: 4 MU50

EMDN nomenclature code(s)

L1508REAMERS, REUSABLE

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.