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Accessory Arch

FDA UDI

Class I (US FDA UDI)

by Lifeport, Llc.

Identity

Trade Name
Accessory Arch FDA UDI
Generic Name
Freestanding/bed-attached intravenous pole FDA UDI
Device Name
ASSEMBLY, ACCESSORY ARCH, 30LB PAYLOAD FDA UDI
Model / Reference
ST2-770-01 FDA UDI
Description
ASSEMBLY, ACCESSORY ARCH, 30LB PAYLOAD FDA UDI

Identifiers

Primary DI / UDI-DI
00810050860147 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

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

Yes

FDA UDI

Category: Freestanding/bed-attached intravenous poleStretcher equipment holder

Accessory Arch by Lifeport, Llc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stretcher equipment holder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lifeport, Llc.

Sources (1)

  • FDA UDI 4e1962e9-fbd2-4798-81fe-f82c382a66c3 34 fields · synced May 30, 2026