FDA UDI Not in Commercial Distribution 🇺🇸 United States

HarmonyAIR

DI: 00724995207496 · Model: G-Series Suspension System · STERIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
HarmonyAIR
Primary DI
00724995207496
Version / Model
G-Series Suspension System
Catalog Number
LG00023V
Company Name
STERIS CORPORATION
Labeler DUNS
036985604
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-11-17
Public Version
2
Public Version Date
2026-01-06
Public Version Status
Update
Public Device Record Key
713f7f2e-c547-4d5a-ab96-c0516e91837f
Distribution End Date
2026-01-05

Device Description

The HarmonyAIR G-Series Spindle Dual Light, Accessory G2 is used with the HarmonyAIR G-Series Suspension System.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
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 00724995207496

Customer Contacts