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iCE boom and Pendant

FDA UDI

Class I (US FDA UDI)

by Amico Clinical Solutions Corp

Identity

Trade Name
iCE boom and Pendant FDA UDI
Generic Name
General utility supply system, ceiling-mounted FDA UDI
Device Name
Saturn Series - Single Mount (Rotating) Electric Brake FDA UDI
Model / Reference
iCE - Saturn FDA UDI
Description
Saturn Series - Single Mount (Rotating) Electric Brake FDA UDI

Identifiers

Catalog Number
LP-H-NNNN-R-E FDA UDI
Primary DI / UDI-DI
00684706001655 FDA UDI
FDA Product Code
FQO FDA UDI
GMDN Term
General utility supply system, ceiling-mounted FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4960 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General utility supply system, ceiling-mounted

iCE boom and Pendant by Amico Clinical Solutions Corp — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General utility supply system, ceiling-mounted.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 251eba48-4e9d-44c9-b943-f1e01ee02ac7 36 fields · synced May 30, 2026