Silicone Vac-Drain Kit

FDA UDI

Class I (US FDA UDI)

by Fortune Medical Instrument Corp.

Identity

Trade Name: Silicone Vac-Drain Kit FDA UDI
Generic Name: Closed-wound drain, non-bioabsorbable FDA UDI
Model / Reference: 2014-9419 FDA UDI

Identifiers

Primary DI / UDI-DI: 14710961935411 FDA UDI
FDA Product Code: GCD FDA UDI
GMDN Term: Closed-wound drain, non-bioabsorbable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4200 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

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: Closed-wound drain, non-bioabsorbable

Silicone Vac-Drain Kit by Fortune Medical Instrument Corp. — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Fortune Medical Instrument Corp.

Sources (1)

FDA UDI 7e628744-1a89-4053-9763-e5cd089bb8c7 32 fields · synced Jun 8, 2026