Tower Assembly

FDA UDI

Class I (US FDA UDI)

by Lifeport, Llc.

Identity

Trade Name: Tower Assembly FDA UDI
Generic Name: Desk mount FDA UDI
Device Name: TOWER ASSEMBLY (ST2-245-03-A2B1C1D1) (00810050860970 has been replaced by 00810050861076) FDA UDI
Model / Reference: 00810050860970 FDA UDI
Description: TOWER ASSEMBLY (ST2-245-03-A2B1C1D1) (00810050860970 has been replaced by 00810050861076) FDA UDI

Identifiers

Primary DI / UDI-DI: 00810050860970 FDA UDI
FDA Product Code: FOX FDA UDI
GMDN Term: Desk mount 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Desk mount

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Lifeport, Llc.

Sources (1)

FDA UDI d4d0a507-0fde-4e8c-9d94-f1c638691023 34 fields · synced Jun 8, 2026