FDA UDI Not in Commercial Distribution 🇺🇸 United States

GE Healthcare

DI: 10009336009166 · Model: 2106917-001 · GRAPHIC CONTROLS ACQUISITION CORP
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
60

Basic Information

Brand Name
GE Healthcare
Primary DI
10009336009166
Version / Model
2106917-001
Catalog Number
2106917-001
Company Name
GRAPHIC CONTROLS ACQUISITION CORP
Labeler DUNS
002111896
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
60
Record Status
Published
Publish Date
2018-04-12
Public Version
3
Public Version Date
2021-05-24
Public Version Status
Update
Public Device Record Key
50ea47db-a2f9-40b4-9feb-480c24e252ed
Distribution End Date
2021-05-24

Device Description

Electrode

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
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
DRX Electrode, Electrocardiograph

GMDN Terms

Code Name
35035 Electrocardiographic electrode, single-use

Identifiers

Type ID
Package 50009336009164
Primary 10009336009166
Unit of Use 00009336009169

Customer Contacts