FDA UDI In Commercial Distribution 🇺🇸 United States

BlueSensor NECG Electrodes

DI: 05707480025893 · Model: N-00-F/25 · Ambu A/S
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
25

Basic Information

Brand Name
BlueSensor NECG Electrodes
Primary DI
05707480025893
Version / Model
N-00-F/25
Catalog Number
N-00-F/25
Company Name
Ambu A/S
Labeler DUNS
305682023
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2016-09-21
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
111d1699-2845-4cfd-8896-ddc99c749191

Device Description

ECG Electrodes Wet Gel F Fitting

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 05707480025886
Primary 05707480025893
Package 05707480003495
Unit of Use 05707480025909

Customer Contacts

Phone
+14107686464

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 25 Degrees Celsius