Identity
- Trade Name
- 35X10 IVF PETRIDISH NONTREATED VENTS FDA UDI
- Generic Name
- Assisted reproduction procedure dish FDA UDI
- Model / Reference
- 150255 FDA UDI
Identifiers
- Catalog Number
- 150255 FDA UDI
- Primary DI / UDI-DI
- 05713311000045 FDA UDI
- FDA Product Code
- PUD FDA UDI
- GMDN Term
- Assisted reproduction procedure dish FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.6160 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
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
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
35x10 Ivf Petridish Nontreated Vents by Nunc A/S — 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
- Nunc A/S
Sources (1)
- FDA UDI 75b34bea-1bd1-4fca-889a-8d3e86fd1f0e 35 fields · synced Jun 8, 2026