Identity
- Trade Name
- STEEN Solution™ FDA UDI
- Generic Name
- Donor-organ/tissue/cell preservation solution FDA UDI
- Device Name
- STEEN Solution™ is intended for assessment of isolated lungs after removal from the donor body for eventual transplantation into a recipient. FDA UDI
- Model / Reference
- 19004 FDA UDI
- Description
- STEEN Solution™ is intended for assessment of isolated lungs after removal from the donor body for eventual transplantation into a recipient. FDA UDI
Identifiers
- Catalog Number
- 19004 FDA UDI
- Primary DI / UDI-DI
- 07350069520036 FDA UDI
- FDA Product Code
- PHO FDA UDI
- GMDN Term
- Donor-organ/tissue/cell preservation solution FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 500 Milliliter FDA UDI
Category: Donor-organ/tissue/cell preservation solution
STEEN Solution™ by Xvivo Perfusion, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Donor-organ/tissue/cell preservation solution.
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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 III | Pending data |
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Manufacturer
- Manufacturer
- Xvivo Perfusion, Inc.
Sources (1)
- FDA UDI 84479154-6838-4d0b-809b-8c0f27a78162 37 fields · synced Jun 20, 2026