Identity
- Trade Name
- Sydney IVF FDA UDI
- Generic Name
- IVF medium kit FDA UDI
- Device Name
- SYDNEY IVF, BLASTOCYST MEDIUM FDA UDI
- Model / Reference
- G46296 FDA UDI
- Description
- SYDNEY IVF, BLASTOCYST MEDIUM FDA UDI
Identifiers
- Catalog Number
- K-SIBM-20-AA FDA UDI
- Primary DI / UDI-DI
- 00827002462960 FDA UDI
- FDA Product Code
- MQL FDA UDI
- GMDN Term
- IVF medium kit 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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Sydney IVF by William A. Cook Australia Pty. Ltd. — 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
- William A. Cook Australia Pty. Ltd.
Sources (1)
- FDA UDI 3fe61149-ec54-4d03-ab78-14a2b5e5d654 37 fields · synced May 31, 2026