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96000-Hh

EUDAMED

Class I (EU MDR)

Ref 96000-HHModel 93050, 93050A, 93050B, 93050C, 93050CW, 93050D, 93050J, 93050K,96000, 96000A, 96000B, 96000C, 96000CA, 96000J, 96000K, 96000L,95000A, 95000L, 95000M, 95000N, 95000MV, 95000TG

by Miraclean Technology Co., Ltd

Identity

Model / Reference
93050, 93050A, 93050B, 93050C, 93050CW, 93050D, 93050J, 93050K,96000, 96000A, 96000B, 96000C, 96000CA, 96000J, 96000K, 96000L,95000A, 95000L, 95000M, 95000N, 95000MV, 95000TG EUDAMED
96000-HH EUDAMED

Identifiers

Primary DI / UDI-DI
06971893323283 EUDAMED
Basic UDI-DI
697189332ZRDSS005TY EUDAMED
EMDN Code
A1101 SAMPLE COLLECTION NEUTRAL SWABS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

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: General-purpose absorbent tip applicator/swab, single-use

96000-Hh by Miraclean Technology Co., Ltd. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose absorbent tip applicator/swab, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000011683
Authorised Representative
Share info GmbH DE-AR-000005132

Sources (1)

  • EUDAMED 4e949008-9eaa-494f-aeec-6ecd148412cd 61 fields · synced Jun 17, 2026