Market Intelligence

Turkey

Medical device market intelligence for Turkey. Regulatory changes, competitor moves, and procurement trends.

122
Signals / 7 days
338
Activity Score
TITCK
TITCK Registration · CE Marking (accepted)

Recent signals

reg_registration2026-06-03

The Unimag Surgical Brain Pad by UNI MAG is classified as a Class III medical device with UDI-DI 08699909793865.

EUDAMED EU Device Database ·
reg_registration2026-06-03

The Unimag Surgical Brain Pad is a Class III medical device registered by UNI MAG TIBBİ VE KİMYASAL MALZEMELER SAN.

EUDAMED EU Device Database ·
reg_registration2026-06-01

Mikron Makina Sanayi ve Ticaret Ltd. Sti. is registered with the FDA under product code HWK.

FDA Device Registration & Listing ·
reg_registration2026-05-31

The SO MATRIX device by İstem Medikal is classified as Class III and registered under UDI-DI 08699415733638.

EUDAMED EU Device Database ·
reg_registration2026-05-31

The SO MATRIX device by İstem Medikal is classified as Class III and registered in EUDAMED.

EUDAMED EU Device Database ·
reg_registration2026-05-31

The SO MATRIX device by İstem Medikal is classified as Class III and registered in EUDAMED.

EUDAMED EU Device Database ·
reg_registration2026-05-31

The SO MATRIX device by İstem Medikal is classified as Class III and registered in EUDAMED.

EUDAMED EU Device Database ·
reg_registration2026-05-31

The SO MATRIX device by İstem Medikal is classified as Class III and has a UDI-DI of 08699415733669.

EUDAMED EU Device Database ·
reg_enforcement2026-05-29

A PMCF study is recruiting 561 patients to evaluate METROSAN spinal systems and BONEGRAFT materials for safety and effectiveness.

ClinicalTrials.gov · 2026-04-27
reg_registration2026-05-27

The HYDROTOUCH device by İstem Medikal is classified as Class IIA and registered with UDI-DI 18699415733918.

EUDAMED EU Device Database ·
reg_registration2026-05-26

The Dolphin device by BURSA PAZARI is classified as Class I and registered in EUDAMED.

EUDAMED EU Device Database ·
reg_registration2026-05-26

The ipekdental device by İPEKDENT MEDİKAL is classified as Class IIA and registered under UDI-DI 08684531701265.

EUDAMED EU Device Database ·
reg_registration2026-05-25

Cardimed Asia Medikal Sanayi ve Ticaret Ltd Sti is registered with the FDA under product code GCJ.

FDA Device Registration & Listing ·
reg_registration2026-05-25

GoldCath by DEMERSAN is classified as Class IIa medical device in EUDAMED with UDI-DI 08680110403551.

EUDAMED EU Device Database ·
reg_registration2026-05-25

The GoldCath device by DEMERSAN is classified as Class IIa and registered in EUDAMED.

EUDAMED EU Device Database ·
reg_registration2026-05-25

GoldCath by DEMERSAN is registered as a Class IIa medical device in EUDAMED.

EUDAMED EU Device Database ·
reg_registration2026-05-25

GoldCath by Demersan is registered as a Class IIA medical device in EUDAMED.

EUDAMED EU Device Database ·
reg_registration2026-05-24

GoldCath by DEMERSAN is registered as a Class IIa medical device in EUDAMED.

EUDAMED EU Device Database ·
reg_registration2026-05-19

IVUS ILAC SANAYI VE TICARET AS has registered two medical devices with product code MVN.

FDA Device Registration & Listing ·
reg_registration2026-05-17

The Oltho device by SELES SAGLIK is classified as Class IIB and has a UDI-DI of 08682431301615.

EUDAMED EU Device Database ·

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