FDA UDI In Commercial Distribution 🇺🇸 United States

HarmonyAIR

DI: 00724995166229 · Model: M-Series Suspension · STERIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
HarmonyAIR
Primary DI
00724995166229
Version / Model
M-Series Suspension
Catalog Number
LM0004
Company Name
STERIS CORPORATION
Labeler DUNS
036985604
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-15
Public Version
2
Public Version Date
2021-01-27
Public Version Status
Update
Public Device Record Key
f6fe1c80-5463-4c52-ba95-7a11b31d817d

Device Description

The Packages Spindle 10065552 M-Series is used with the HarmonyAIR M-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 00724995166229

Customer Contacts