FDA UDI In Commercial Distribution 🇺🇸 United States

Baxter

DI: 20185098000843 · Model: Baxter-022 · PRO MEDICAL SUPPLIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1600

Basic Information

Brand Name
Baxter
Primary DI
20185098000843
Version / Model
Baxter-022
Catalog Number
Baxter-022
Company Name
PRO MEDICAL SUPPLIES, INC.
Labeler DUNS
135741127
Distribution Status
In Commercial Distribution
Device Count in Pkg
1600
Record Status
Published
Publish Date
2016-08-24
Public Version
4
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
febd96b7-c0e2-4f5a-9426-e40c229b4344

Device Description

(1600) Baxter Electrodes 2.0"x2.0" Black Foam (400 packs per case - 4 electrodes per pack = 1600 pieces)

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GXY Electrode, Cutaneous

GMDN Terms

Code Name
35995 Transcutaneous electrical stimulation electrode, single-use

Identifiers

Type ID
Primary 20185098000843
Unit of Use 18509800084916

Customer Contacts

Phone
215-938-0200

Premarket Submissions

Submission Number Supplement Number
K132998 000