Identity
- Trade Name
- YSI Incorporated FDA UDI
- Generic Name
- Buffered sample diluent IVD FDA UDI
- Device Name
- 2357 BUFFER KIT FDA UDI
- Model / Reference
- 2357 FDA UDI
- Description
- 2357 BUFFER KIT FDA UDI
Identifiers
- Catalog Number
- 098005 FDA UDI
- Primary DI / UDI-DI
- 00851683007165 FDA UDI
- FDA Product Code
- CGA FDA UDI
- GMDN Term
- Buffered sample diluent IVD FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1345 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Buffered sample diluent IVD
YSI Incorporated by Ysi Incorporated — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Ysi Incorporated
Sources (1)
- FDA UDI 6c1eabdd-5bb4-4111-893e-5daf03404012 34 fields · synced May 29, 2026