Identity
- Trade Name
- ultraView Red ISH DIG Detection Kit FDA UDI
- Generic Name
- Nucleic acid hybridization detection IVD, kit FDA UDI
- Model / Reference
- 100 tests FDA UDI
Identifiers
- Catalog Number
- 05587778001 FDA UDI
- Primary DI / UDI-DI
- 04015630970391 FDA UDI
- FDA Product Code
- PPM FDA UDI
- GMDN Term
- Nucleic acid hybridization detection IVD, kit FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.4010 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
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Nucleic acid hybridization detection IVD, kit
ultraView Red ISH DIG Detection Kit by Ventana Medical Systems — 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
- Ventana Medical Systems
Sources (1)
- FDA UDI ca643ac6-d3c6-4f2f-b218-f3571a6147e1 33 fields · synced Jun 1, 2026