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Mcintosh Blade, Fig. 2
EUDAMEDClass I (EU MDR)
Ref 03-010-02Model 03-005-40 to 03-030-15
Identity
- Trade Name
- MCINTOSH BLADE, FIG. 2 EUDAMED
- Device Name
- Anesthesia Instruments EUDAMED
- Model / Reference
- 03-005-40 to 03-030-15 EUDAMED03-010-02 EUDAMED
Identifiers
- Primary DI / UDI-DI
- +G16403020010V EUDAMED
- Basic UDI-DI
- ++G1640300540to302R2 EUDAMED
- EMDN Code
- R9002 LARYNGOSCOPE BLADES, SINGLE-USE 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
Mcintosh Blade, Fig. 2 by Eltek Instruments Pvt Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | ++G1640300540to302R2 | Class I | Active |
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Manufacturer
- Manufacturer
- Eltek Instruments Pvt Ltd
- EUDAMED SRN
- PK-MF-000024315
- Authorised Representative
- CS Active LV-AR-000011602
Sources (1)
- EUDAMED 3903e888-048c-48ed-b539-fe5e2665da3f 61 fields · synced Jul 25, 2026