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Silicone Sump Drain Tube

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 2016-0314

by Fortune Medical Instrument Corp.

Identity

Trade Name
Silicone Sump Drain Tube EUDAMEDFDA UDI
Generic Name
Sump drain FDA UDI
Device Name
Silicone Sump Drain Tube EUDAMED
Model / Reference
2016-0314 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
14710961935893 EUDAMEDFDA UDI
Basic UDI-DI
B-14710961935893 EUDAMED
FDA Product Code
GBW FDA UDI
EMDN Code
A060206 PERITONAEAL DRAINAGES AND KITS EUDAMED
GMDN Term
Sump drain FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
878.4200 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
TW-MF-000009221
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 6e552f13-ae18-44e4-94cf-a522ccb58437 61 fields · synced May 30, 2026
  • FDA UDI 0f1a219d-9986-426b-b36d-564eeec8e9ec 32 fields · synced May 30, 2026