Identity
- Trade Name
- ECLIPSE Ti2-I US FDA UDI
- Generic Name
- Inverted-stage light microscope FDA UDI
- Model / Reference
- MEA54315 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04549921600341 FDA UDI
- FDA Product Code
- MTX FDA UDI
- GMDN Term
- Inverted-stage light microscope FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 884.6190 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Inverted-stage light microscope
ECLIPSE Ti2-I US by Nikon, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 I | Pending data |
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Manufacturer
- Manufacturer
- Nikon, Inc.
Sources (1)
- FDA UDI af93017b-6b0c-49af-a710-6a944bbb4c87 32 fields · synced May 31, 2026