FDA UDI In Commercial Distribution 🇺🇸 United States

LUMISCOPE

DI: M36867001 · Model: 6700 · GF HEALTH PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
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
LUMISCOPE
Primary DI
M36867001
Version / Model
6700
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
5
Public Version Date
2025-09-24
Public Version Status
Update
Public Device Record Key
cfd3c921-803d-4fdd-bdbd-7b74f582e7ab

Device Description

Portable Ultrasonic Nebulizer

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
CAF Nebulizer (Direct Patient Interface)

GMDN Terms

Code Name
35457 Therapeutic agent nebulizer, benchtop

Identifiers

Type ID
Package M36867003
Package M36867002
Primary M36867001

Customer Contacts

Phone
770-368-4700

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
15 – 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-25 – 55 Degrees Celsius