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Fms

FDA UDI

Class II (US FDA UDI)

by Medos International Sàrl

Identity

Trade Name
FMS FDA UDI
Generic Name
Surgical irrigation tubing set, single-use FDA UDI
Device Name
FMS Fluid Management System Intermediary Tubing with One-way valve FDA UDI
Model / Reference
281142 FDA UDI
Description
FMS Fluid Management System Intermediary Tubing with One-way valve FDA UDI

Identifiers

Catalog Number
281142 FDA UDI
Primary DI / UDI-DI
10886705015900 FDA UDI
510(k) Number
K951843 FDA UDI
FDA Product Code
HRX FDA UDI
GMDN Term
Surgical irrigation tubing set, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical irrigation tubing set, single-use

Fms by Medos International Sàrl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation tubing set, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 11db43f9-2248-460e-8223-2a7dbec2a7b6 37 fields · synced May 31, 2026