Identity
- Trade Name
- Acquicell FDA UDI
- Generic Name
- Stromal vascular fraction recovery unit, multi-modality FDA UDI
- Model / Reference
- MMT-500D FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850421007597 FDA UDI
- FDA Product Code
- GEY FDA UDI
- GMDN Term
- Stromal vascular fraction recovery unit, multi-modality FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4820 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
No
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Stromal vascular fraction recovery unit, multi-modality
Acquicell by Millennium Medical Technologies, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Stromal vascular fraction recovery unit, multi-modality.
- Tissue Processing Unit — InGeneron Inc. · Class I
- Acquicell Pro — Millennium Medical Technologies, 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
- Millennium Medical Technologies, Inc.
Sources (1)
- FDA UDI 2c578744-fcad-4b94-bc62-1b545d96eb10 32 fields · synced May 30, 2026