Sperm Collection Container

FDA UDI

Class II (US FDA UDI)

by Vitrolife Sweden AB

Identity

Trade Name: Sperm Collection Container FDA UDI
Generic Name: Semen specimen collection container FDA UDI
Model / Reference: 16102 FDA UDI

Identifiers

Primary DI / UDI-DI: 07350025914565 FDA UDI
FDA Product Code: PUD FDA UDI
GMDN Term: Semen specimen collection container 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

Yes

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

Category: Semen specimen collection container

Sperm Collection Container by Vitrolife Sweden AB — 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: Vitrolife Sweden AB

Sources (1)

FDA UDI a7291847-409e-444b-9aa9-0cb3ea36b8cc 32 fields · synced Jun 8, 2026