FDA UDI In Commercial Distribution 🇺🇸 United States

BodyMed

DI: 00815991023019 · Model: ZZACOMBO · BOXOUT, LLC
Product Codes
3
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
BodyMed
Primary DI
00815991023019
Version / Model
ZZACOMBO
Catalog Number
ZZACOMBO
Company Name
BOXOUT, LLC
Labeler DUNS
066689993
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-10-31
Public Version
6
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
7abf8028-c478-4d23-9bad-7f77a915836b

Device Description

BODYMED TENS/EMS/MASSAGER COMBO

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IPF Stimulator, Muscle, Powered
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
ISA Massager, Therapeutic, Electric

GMDN Terms

Code Name
46573 Physical therapy transcutaneous neuromuscular electrical stimulation system

Identifiers

Type ID
Package 20815991023013
Package 10815991023016
Primary 00815991023019

Customer Contacts

Phone
866-528-2152

Premarket Submissions

Submission Number Supplement Number
K181688 000