Identity
- Trade Name
- mixsoon Derma Booster PRO FDA UDI
- Generic Name
- Tissue processor IVD, automated/semi-automated FDA UDI
- Device Name
- personal home care facial massage device FDA UDI
- Model / Reference
- mixsoon Derma Booster PRO FDA UDI
- Description
- personal home care facial massage device FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08809732914683 FDA UDI
- FDA Product Code
- ISA FDA UDI
- GMDN Term
- Tissue processor IVD, automated/semi-automated FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5660 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Tissue processor IVD, automated/semi-automated
mixsoon Derma Booster PRO by Haho Medi — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Tissue processor IVD, automated/semi-automated.
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- Thermo Fisher — SHANDON DIAGNOSTICS LIMITED · Class I
- Leica TP1020 (Single loading) without vacuum/ — Leica Biosystems Nussloch GmbH · Class I
- ASP6025 S 120V/50-60Hz — Leica Biosystems Nussloch GmbH · Class I
- Leica TP1020 (Double loading) Without vaccum/w — Leica Biosystems Nussloch GmbH · Class I
- Tissue-Tek Xpress® — Sakura Finetek USA, Inc · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Haho Medi
Sources (1)
- FDA UDI 4b985928-c1be-4625-bfa8-88eac93a65ef 34 fields · synced May 30, 2026