FDA UDI In Commercial Distribution 🇺🇸 United States

Tempus LS-Manual

DI: 05060472441966 · Model: 01-3022 · REMOTE DIAGNOSTIC TECHNOLOGIES LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Tempus LS-Manual
Primary DI
05060472441966
Version / Model
01-3022
Company Name
REMOTE DIAGNOSTIC TECHNOLOGIES LIMITED
Labeler DUNS
896707940
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-06
Public Version
1
Public Version Date
2020-08-14
Public Version Status
New
Public Device Record Key
286c7c19-5270-49b7-91e9-f9eac64d3123

Device Description

Tempus LS-Manual Securing Pads

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
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
LDD Dc-Defibrillator, Low-Energy, (Including Paddles)

GMDN Terms

Code Name
17882 Physiologic-monitoring defibrillation system

Identifiers

Type ID
Primary 05060472441966

Premarket Submissions

Submission Number Supplement Number
K200849 000