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Upside Down Peri Bottle
EUDAMEDClass I (EU MDR)
Ref K5101EUModel K5101EU, K5102EU
Identity
- Device Name
- Upside Down Peri Bottle EUDAMED
- Model / Reference
- K5101EU, K5102EU EUDAMEDK5101EU EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06970289032006 EUDAMED
- Basic UDI-DI
- 69702890351001YD EUDAMED
- EMDN Code
- U0899 GYNAECOLOGICAL DEVICES - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Austria 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
Upside Down Peri Bottle by Hetaida 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 69702890351001YD | Class I | Active |
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Manufacturer
- Manufacturer
- Hetaida Technology Co., Ltd.
- EUDAMED SRN
- CN-MF-000032793
- Authorised Representative
- SUNGO Europe B.V. NL-AR-000000247
Sources (1)
- EUDAMED dc127907-2f9a-4c3f-91f8-58f744ec5732 61 fields · synced Jun 18, 2026