FDA UDI In Commercial Distribution 🇺🇸 United States

HarmonyAIR

DI: 00724995190255 · Model: A-Series Suspension System · STERIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HarmonyAIR
Primary DI
00724995190255
Version / Model
A-Series Suspension System
Catalog Number
LAS000002
Company Name
STERIS CORPORATION
Labeler DUNS
036985604
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-28
Public Version
2
Public Version Date
2021-01-27
Public Version Status
Update
Public Device Record Key
506ba0ec-2767-4748-9894-6457dadb5982

Device Description

The A-Series Spindle Triple Light is used with the HarmonyAIR A-Series Suspension System.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FQO TABLE, OPERATING-ROOM, AC-POWERED

GMDN Terms

Code Name
32245 Medical monitor/light mount

Identifiers

Type ID
Primary 00724995190255

Customer Contacts