FDA UDI In Commercial Distribution 🇺🇸 United States

LUMISCOPE

DI: M3681000211 · Model: 100-021 · GF HEALTH PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
LUMISCOPE
Primary DI
M3681000211
Version / Model
100-021
Company Name
GF HEALTH PRODUCTS, INC.
Labeler DUNS
132016168
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-31
Public Version
4
Public Version Date
2019-07-25
Public Version Status
Update
Public Device Record Key
f93c138d-e822-457a-a9eb-51b07eb6dadb

Device Description

Self Taking Blood Pressure Kit

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DXQ Blood Pressure Cuff

GMDN Terms

Code Name
16156 Aneroid manual sphygmomanometer

Identifiers

Type ID
Package M3681000213
Package M3681000212
Primary M3681000211

Customer Contacts

Phone
770-368-4700

Premarket Submissions

Submission Number Supplement Number
K092245 000

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
– 85 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-20 – 50 Degrees Celsius