Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ 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.

Organization name
UDI-DI code
Reference / catalog number

Ø2 mm drill stop - short 10 /… — Class I MDR by DEEP Company

MD Atlas
DEEP Company

EUDAMED last updated this device on Mar 25, 2026

Ø2 mm drill stop - short 10 / long 14

3665588BUTEE200AQ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: DEEP Company
UDI-DI code: 03665588007499
Reference / catalog number: PFD30-I92032014

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?

Manufacturer information

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

Related devices

Countersink - 4 mm diameter3665588COUNT200EWOn the market 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

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 25, 2026

Device identification

Trade name: Ø2 mm drill stop - short 10 / long 14
UDI-DI code: 03665588007499
Basic UDI-DI: 3665588BUTEE200AQ
Reference / catalog number: PFD30-I92032014
Issuing entity: GS1

Classification

Risk category: Class I
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: No clinical sizes registered for this device.

EMDN nomenclature code(s)

L159099ODONTOSTOMATOLOGY INSTRUMENTS, REUSABLE - OTHER

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.