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Skytron

FDA UDI

Class I (US FDA UDI)

by Skytron, LLC

Identity

Trade Name
Skytron FDA UDI
Generic Name
Freestanding/bed-attached intravenous pole FDA UDI
Device Name
STRYKER IN-TOUCH BED MOUNT 20.5 Inch ARM W/5 Inch CASTER AND 20.5 Inch TELESCOPING ARM FDA UDI
Model / Reference
SYK-IT-L Streamline FDA UDI
Description
STRYKER IN-TOUCH BED MOUNT 20.5 Inch ARM W/5 Inch CASTER AND 20.5 Inch TELESCOPING ARM FDA UDI

Identifiers

Catalog Number
SYK-IT-L FDA UDI
Primary DI / UDI-DI
10841736118723 FDA UDI
FDA Product Code
FOX FDA UDI
GMDN Term
Freestanding/bed-attached intravenous pole FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6990 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Freestanding/bed-attached intravenous pole

Skytron by Skytron, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Freestanding/bed-attached intravenous pole.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Skytron, LLC

Sources (1)

  • FDA UDI ca19e220-e0b9-4d3b-9066-377bf60fddd4 35 fields · synced Jun 8, 2026