Silicone Hubless Endo Drain Kit with Bendable Trocar

FDA UDI

Class I (US FDA UDI)

by Fortune Medical Instrument Corp.

Identity

Trade Name: Silicone Hubless Endo Drain Kit with Bendable Trocar FDA UDI
Generic Name: Closed-wound drain, non-bioabsorbable FDA UDI
Model / Reference: 2015-9710B FDA UDI

Identifiers

Primary DI / UDI-DI: 14711182606548 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 Hubless Endo Drain Kit with Bendable Trocar by Fortune Medical Instrument Corp. — Class I — FDA UDI — listed in FDA GUDID

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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 6bfb4e8a-8109-4022-a461-80a89e1f7598 32 fields · synced May 31, 2026