← Back to catalogue

FloSteady

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
FloSteady FDA UDI
Generic Name
Surgical irrigation/aspiration tubing set FDA UDI
Device Name
[Arthroscopy Pump, Do not use if package is damaged, Keep dry, Keep away from sunlight, Protect from heat and radioactive sources.] FDA UDI
Model / Reference
0350800006 FDA UDI
Description
[Arthroscopy Pump, Do not use if package is damaged, Keep dry, Keep away from sunlight, Protect from heat and radioactive sources.] FDA UDI

Identifiers

Catalog Number
0350-800-006 FDA UDI
Primary DI / UDI-DI
07613327061680 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

FloSteady 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 05f3edb3-ef65-40af-b656-e692786baf39 35 fields · synced May 30, 2026