Identity
- Trade Name
- Tyrode's Solution - Acidified FDA UDI
- Generic Name
- Assisted reproduction microtool FDA UDI
- Device Name
- Tyrode's Solution - Acidified FDA UDI
- Model / Reference
- 99252-12X5ML FDA UDI
- Description
- Tyrode's Solution - Acidified FDA UDI
Identifiers
- Catalog Number
- 99252 FDA UDI
- Primary DI / UDI-DI
- 00893727002996 FDA UDI
- 510(k) Number
- K991339 FDA UDI
- FDA Product Code
- MQL FDA UDI
- GMDN Term
- Assisted reproduction microtool FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.6180 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 5 Milliliter FDA UDI
Tyrode's Solution - Acidified by Fujifilm Irvine Scientific, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Fujifilm Irvine Scientific, Inc.
Sources (1)
- FDA UDI 3e540c11-6332-4d45-8379-a0bfdf63186d 39 fields · synced May 29, 2026