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Silicone Round Drain

FDA UDIEUDAMED

Class I (US FDA UDI)

by Fortune Medical Instrument Corp.

Identity

Trade Name
Silicone Round Drain FDA UDI
Generic Name
Closed-wound drain, non-bioabsorbable FDA UDI
Model / Reference
2015-0308 FDA UDI

Identifiers

Primary DI / UDI-DI
14710961935671 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

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Closed-wound drain, non-bioabsorbable

Silicone Round Drain by Fortune Medical Instrument Corp. — Class I — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Closed-wound drain, non-bioabsorbable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 3648b9cd-76ed-47dd-b1b8-501aa44c6b8d 32 fields · synced Jun 19, 2026
  • EUDAMED 1 fields · synced Jun 3, 2026