Identity
- Trade Name
- RI Witness FDA UDI
- Generic Name
- Assisted reproduction electromechanical micromanipulator FDA UDI
- Device Name
- Assisted Reproduction Accessories FDA UDI
- Model / Reference
- Embryology Heated Plate FDA UDI
- Description
- Assisted Reproduction Accessories FDA UDI
Identifiers
- Catalog Number
- 6-70-807 FDA UDI
- Primary DI / UDI-DI
- 05060170185834 FDA UDI
- 510(k) Number
- K160504 FDA UDI
- FDA Product Code
- MQG FDA UDI
- GMDN Term
- Assisted reproduction electromechanical micromanipulator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.6120 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
Yes
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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Assisted reproduction electromechanical micromanipulator
RI Witness by Research Instruments , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K160504 also covers:
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 II | Pending data |
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Manufacturer
- Manufacturer
- Research Instruments , Ltd.
Sources (1)
- FDA UDI 0531e360-694e-49dc-98f3-2b626d564d00 36 fields · synced May 31, 2026