Identity
- Trade Name
- Neodisher® GK FDA UDI
- Generic Name
- Wash/cleaning solution IVD, manual equipment FDA UDI
- Device Name
- Cleaning agent for laboratory use FDA UDI
- Model / Reference
- 10446123 FDA UDI
- Description
- Cleaning agent for laboratory use FDA UDI
Identifiers
- Catalog Number
- OQRK51 FDA UDI
- Primary DI / UDI-DI
- 00842768008009 FDA UDI
- FDA Product Code
- JCB FDA UDI
- GMDN Term
- Wash/cleaning solution IVD, manual equipment 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
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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Wash/cleaning solution IVD, manual equipment
Neodisher® GK by Siemens Healthcare Diagnostics Products Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Wash/cleaning solution IVD, manual equipment.
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
- Siemens Healthcare Diagnostics Products Ltd
Sources (1)
- FDA UDI 7535ee9b-0654-4ed3-b71f-94523d0ce2d7 36 fields · synced May 30, 2026