Single-use Laryngoscope Blade

EUDAMED

Class I (EU MDR)

Ref HS P2Model HS 2,HS 3,HS 4,HS M3,HS M4,HS P2,HS ML0

by Shenzhen HugeMed Medical Technical Development Co., Ltd.

Identity

Device Name: Single-use Laryngoscope Blade EUDAMED
Model / Reference: HS 2,HS 3,HS 4,HS M3,HS M4,HS P2,HS ML0 EUDAMED
HS P2 EUDAMED

Identifiers

Primary DI / UDI-DI: 06970462542476 EUDAMED
Basic UDI-DI: 69704625421057S EUDAMED
EMDN Code: R9002 LARYNGOSCOPE BLADES, SINGLE-USE EUDAMED

Classification

Device Class: Class I EUDAMED
Market of Registration: Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

EUDAMED

Reusable

EUDAMED

Contains Latex

EUDAMED

Reprocessed

EUDAMED

CMR Substance

EUDAMED

Human-derived

EUDAMED

Human Tissues

EUDAMED

Animal Tissues

EUDAMED

Endocrine Disruptor

EUDAMED

Administering Medicine

EUDAMED

Measuring Function

EUDAMED

Incorporates Medicinal Product

EUDAMED

Single-use Laryngoscope Blade by Shenzhen HugeMed Medical Technical Development Co., 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	69704625421057S	Class I	Active

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Manufacturer

Manufacturer: Shenzhen HugeMed Medical Technical Development Co., Ltd.
EUDAMED SRN: CN-MF-000010895
Authorised Representative: Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

EUDAMED 1ce29c73-3c65-4dfc-8735-1e5530dd1228 61 fields · synced Jun 18, 2026