FDA UDI In Commercial Distribution 🇺🇸 United States

DRIVEMEDICAL

DI: 00822383985718 · Model: RTLAGF-1010 · Drive Devilbiss Healthcare
Product Codes
1
GMDN Terms
4
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
DRIVEMEDICAL
Primary DI
00822383985718
Version / Model
RTLAGF-1010
Company Name
Drive Devilbiss Healthcare
Labeler DUNS
867673159
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-16
Public Version
7
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
ae051079-f023-49d8-9dbf-eb4ececb1528

Device Description

ElectrotherapyAccessories Product Description: Electrode Pk 1LG/1SM, For RTLAGF-1000

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
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
GXY ELECTRODE, CUTANEOUS

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system
35751 Transcutaneous electrical stimulation lead
35372 Analgesic transcutaneous electrical nerve stimulation system
35995 Transcutaneous electrical stimulation electrode, single-use

Identifiers

Type ID
Package 50822383985713
Package 10822383985715
Primary 00822383985718