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Create Biotech Co., Ltd.

Active in EUDAMED

Taiwanfrom SRN EUDAMED FDA SRN TW-MF-000021770 FEI 3016734145

Devices
138
Registrations
EUDAMEDFDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA FEI

What Create Biotech Co., Ltd. makes

Create Biotech Co., Ltd. manufactures tracheal tube introducers, which assist in the insertion of endotracheal tubes during medical procedures.

These devices are classified as Class IIa under EU regulations and are listed in the EUDAMED registry. The company is based in Taiwan.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue138

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Company details

EUDAMED SRN
TW-MF-000021770
FDA FEI number
3016734145
DUNS number
656387282
EUDAMED status
Active
EUDAMED registered name
Create Biotech Co., Ltd.
Registered address
NO.68, GONG 7TH RD., LONGTAN DIST.,, 32559, TAOYUAN CITY, Taiwan
Phone
+88634090045
PRRC contact
Chen-Yu Jen(public in EUDAMED)

Frequently asked questions

How many devices does CREATE BIOTECH CO., LTD. have in the registry?

The registry currently lists 138 devices for CREATE BIOTECH CO., LTD.. Devices recorded under merged duplicate company entries are counted once.

Which registries list CREATE BIOTECH CO., LTD.'s devices?

Among its 50 most recently registered devices, CREATE BIOTECH CO., LTD. has devices listed in EUDAMED (16 devices) and FDA GUDID (34 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do CREATE BIOTECH CO., LTD.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for CREATE BIOTECH CO., LTD.'s devices are Class I and Class IIa. Each device page shows its own class and authorisation.

What are the newest devices from CREATE BIOTECH CO., LTD. in the registry?

The most recently registered devices listed for CREATE BIOTECH CO., LTD. include Breathing System Filter, Breathing Circuit, Tracheal Tube Introducer and Create Biotech 016-009-003.

Generated automatically from registry data and not verified by a human reviewer.