FDA UDI Not in Commercial Distribution 🇺🇸 United States

Ambu WhiteSensor 5050

DI: 05707480141289 · Model: 5050-00-S/3 · Ambu A/S
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
3

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Basic Information

Brand Name
Ambu WhiteSensor 5050
Primary DI
05707480141289
Version / Model
5050-00-S/3
Catalog Number
5050-00-S/3
Company Name
Ambu A/S
Labeler DUNS
305682023
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
3
Record Status
Published
Publish Date
2019-06-03
Public Version
3
Public Version Date
2026-01-30
Public Version Status
Update
Public Device Record Key
8563dac1-b41d-4680-897c-a1e965d5d5a0
Distribution End Date
2020-09-10

Device Description

Ambu WhiteSensor 5050

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 05707480141296
Primary 05707480141289
Package 05707480141302
Unit of Use 05707480141272

Customer Contacts

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
5 – 30 Degrees Celsius