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FloControl, Fluid Safe

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
FloControl, Fluid Safe FDA UDI
Generic Name
Surgical irrigation/aspiration tubing set FDA UDI
Device Name
Arthroscopy Pump, Fluid Management System, Do not use if package is damaged, Keep dry, Keep away from sunlight, Protect from heat and radioactive sources. FDA UDI
Model / Reference
0350202000 FDA UDI
Description
Arthroscopy Pump, Fluid Management System, Do not use if package is damaged, Keep dry, Keep away from sunlight, Protect from heat and radioactive sources. FDA UDI

Identifiers

Catalog Number
0350-202-000 FDA UDI
Primary DI / UDI-DI
07613327061710 FDA UDI
FDA Product Code
HRX FDA UDI
GMDN Term
Surgical irrigation/aspiration tubing set 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/aspiration tubing set

FloControl, Fluid Safe by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation/aspiration tubing set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI b01db2ee-15c9-48d4-9e8f-a0e2e31cc2ce 35 fields · synced May 30, 2026