AT-Patch

GUDID 18800069700175

ATsens Co., Ltd.

Electrocardiographic long-term ambulatory recording analyser
Primary Device ID18800069700175
NIH Device Record Key699f9b54-9fb3-4196-bd88-92a89b0a86d7
Commercial Distribution Discontinuation2025-10-31
Commercial Distribution StatusNot in Commercial Distribution
Brand NameAT-Patch
Version Model NumberATP-C130
Company DUNS694967215
Company NameATsens Co., Ltd.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numbertrue
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108800069700178 [Primary]
GS118800069700175 [Package]
Contains: 08800069700178
Package: [10 Units]
Discontinued: 2025-10-31
Not in Commercial Distribution
GS128800069700172 [Package]
Package: [8 Units]
Discontinued: 2025-10-31
Not in Commercial Distribution

FDA Product Code

DSHRecorder, Magnetic Tape, Medical

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2025-11-28
Device Publish Date2022-12-23

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