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Dutau® Novatech®

EUDAMEDFDA UDIFDA 510(k)

Class IIa (EU MDR)

Ref 02BRD1120

by Novatech Sa

Identity

Trade Name
DUTAU NOVATECH FDA UDI
Generic Name
Rigid optical bronchoscope FDA UDI
Device Name
DUTAU® NOVATECH® EUDAMED
Lateral double port FDA UDI
Model / Reference
02BRD1120 EUDAMEDFDA UDI
Description
Lateral double port FDA UDI

Identifiers

Primary DI / UDI-DI
14063108105230 EUDAMEDFDA UDI
Basic UDI-DI
4063108DUTA4 EUDAMED
Direct Marketing DI
14063108105230 EUDAMED
510(k) Number
K242324 FDA UDI
FDA Product Code
EOQ FDA UDI
EMDN Code
Z12020801 BRONCHOSCOPES EUDAMED
GMDN Term
Rigid optical bronchoscope FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
874.4680 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dutau® Novatech® by Novatech Sa — Class IIa — FDA_510K, MDR — listed in EUDAMED, FDA GUDID, FDA 510(k) — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Novatech Sa
EUDAMED SRN
FR-MF-000001658

Sources (3)

  • EUDAMED 9867d377-ec29-4f76-a43d-f6cad85687b7 61 fields · synced Jun 18, 2026
  • FDA UDI 3e3f2fa9-eccf-40b7-b34e-95e5ab4af12d 34 fields · synced May 30, 2026
  • FDA 510(k) K242324 1 fields · synced May 18, 2026