FDA UDI In Commercial Distribution 🇺🇸 United States

IQ SENSOR ALARM 10/CA

DI: 00733657286069 · Model: 71098510 · ALIMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
IQ SENSOR ALARM 10/CA
Primary DI
00733657286069
Version / Model
71098510
Catalog Number
2970008689
Company Name
ALIMED, INC.
Labeler DUNS
056007248
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2022-12-01
Public Version
3
Public Version Date
2024-02-26
Public Version Status
Update
Public Device Record Key
54c7d965-18e8-4362-9d44-b37e8ea42e1d

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
Yes
Has Serial Number
No
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
KMI MONITOR, BED PATIENT

GMDN Terms

Code Name
30087 Vulnerable patient home alert system

Identifiers

Type ID
Primary 00733657286069
Unit of Use 00733657300291

Customer Contacts

Phone
+1(781)329-2900 ext. 0