Nunc Ivf Multidish 4 Well Nunclon

FDA UDI

Class II (US FDA UDI)

by Nunc A/S

Identity

Trade Name: NUNC IVF MULTIDISH 4 WELL NUNCLON FDA UDI
Generic Name: Assisted reproduction procedure dish FDA UDI
Device Name: NUNC IVF MULTIDISH 4 WELL NUNCLON FDA UDI
Model / Reference: 144444 FDA UDI
Description: NUNC IVF MULTIDISH 4 WELL NUNCLON FDA UDI

Identifiers

Primary DI / UDI-DI: 15713311000127 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: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Radiation Sterilization FDA UDI

Category: Assisted reproduction procedure dish

Nunc Ivf Multidish 4 Well Nunclon by Nunc A/S — 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: Nunc A/S

Sources (1)

FDA UDI adf8dfa1-14c0-4f98-bc9a-20e323ed6d5b 33 fields · synced May 30, 2026