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Heat-Sealing Sterilization Flat (gusseted)reel

EUDAMED

Class I (EU MDR)

Ref N/AModel PMDHR: 06975784902113

by Anhui Puremed Medical Technology Co., Ltd

Identity

Device Name
HEAT-SEALING STERILIZATION FLAT (GUSSETED)REEL EUDAMED
Model / Reference
PMDHR: 06975784902113 EUDAMED
N/A EUDAMED

Identifiers

Primary DI / UDI-DI
06975784902113 EUDAMED
Basic UDI-DI
697578490PMSRYG EUDAMED
EMDN Code
S01010101,S01010102,S01010201,S01010301 EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

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

Heat-Sealing Sterilization Flat (gusseted)reel by Anhui Puremed Medical Technology 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

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Manufacturer

EUDAMED SRN
CN-MF-000029249
Authorised Representative
Sungo Cert GmbH DE-AR-000010869

Sources (1)

  • EUDAMED 19f2bbf1-17ec-4f76-abba-df057e246937 61 fields · synced Jun 18, 2026