FDA UDI In Commercial Distribution 🇺🇸 United States

AT-Patch

DI: 08800069700277 · Model: ATP-C70 · ATsens Co., Ltd.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AT-Patch
Primary DI
08800069700277
Version / Model
ATP-C70
Company Name
ATsens Co., Ltd.
Labeler DUNS
696621857
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-11-05
Public Version
2
Public Version Date
2025-11-14
Public Version Status
Update
Public Device Record Key
50fcc11c-1fa0-46cc-8975-fc916566e533

Device Description

The device is intended to measure, analyze, edit and report continuous electrocardiogram (ECG) information for longterm recording (ATP-C130: up to 14 days, ATP-C70: up to 7 days) by attaching to the patient’s torso. ECG records are saved in the device during use and are not intended for real-time monitoring. After the wear period is completed, the ECG data is transmitted to the AT-Report. A primary analysis is performed by the algorithms within the AT-Report, and then a physician report is issued based on those results after a secondary analysis by a clinician or trained operator with experience in ECG analysis to correct any incorrectly detected events. The Physician report is offered to clinicians or physicians on an advisory basis only.

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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
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
DSH Recorder, Magnetic Tape, Medical
DQK Computer, Diagnostic, Programmable
MLO Electrocardiograph, Ambulatory, With Analysis Algorithm

GMDN Terms

Code Name
36827 Electrocardiographic long-term ambulatory recording analyser

Identifiers

Type ID
Primary 08800069700277

Premarket Submissions

Submission Number Supplement Number
K242583 000