← Back to catalogue

Skytron Streamline Boom Adapter

FDA UDI

Class I (US FDA UDI)

by Skytron, LLC

Identity

Trade Name
Skytron Streamline Boom Adapter FDA UDI
Generic Name
Freestanding/bed-attached intravenous pole FDA UDI
Device Name
Streamline Boom Adapter Mount, Fits 36" or 48" Carriers, Ergon 2/3 FDA UDI
Model / Reference
ISS-BOOM FDA UDI
Description
Streamline Boom Adapter Mount, Fits 36" or 48" Carriers, Ergon 2/3 FDA UDI

Identifiers

Primary DI / UDI-DI
10841736113995 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

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

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 Streamline Boom Adapter 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

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

Manufacturer

Manufacturer
Skytron, LLC

Sources (1)

  • FDA UDI 10f1dd78-9fe4-49cd-aaec-e1f855286360 34 fields · synced Jun 6, 2026