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Mcintosh Laryngoscope Set Of 4

EUDAMED

Class I (EU MDR)

Ref 03-005-40Model 03-005-40 to 03-030-15

by Eltek Instruments Pvt Ltd

Identity

Trade Name
MCINTOSH LARYNGOSCOPE SET OF 4 EUDAMED
Device Name
Anesthesia Instruments EUDAMED
Model / Reference
03-005-40 to 03-030-15 EUDAMED
03-005-40 EUDAMED

Identifiers

Primary DI / UDI-DI
+G16403005400. EUDAMED
Basic UDI-DI
++G1640300540to302R2 EUDAMED
EMDN Code
Z12021003 LARYNGOSCOPES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

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

Category: Laryngoscope blade, reusable

Mcintosh Laryngoscope Set Of 4 by Eltek Instruments Pvt Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Laryngoscope blade, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
PK-MF-000024315
Authorised Representative
CS Active LV-AR-000011602

Sources (1)

  • EUDAMED 33a3bd76-df40-4b65-acc1-0ee510260524 61 fields · synced Jul 11, 2026