Otsuka Digital Feedback Device

Primary DI
00857335005114
Brand
Otsuka Digital Feedback Device
Company
Otsuka America Pharmaceutical Inc
Model
Patch
Catalog number
SPC-2731
Device description
The wearable sensor in the Otsuka Digital Feedback Device is a body-worn sensor that consists of a single-use patch known as the D-Tect wearable sensor or D-Tect Patch. The D-Tect Patch collects physiological and behavioral metrics such as heart rate, activity, body angle, and time stamped patient-logged events, including events signaled by the co-incidence with, or co-ingestion with, the ingestible sensor accessory. Note: While the device includes automated heart rate (HR) measurement, it does not provide an ECG waveform recording for display or analysis. The device is not intended to diagnose heart-related conditions and does not include alarms. HR measurement is not intended to be used in alarm system. HR data may not be accurate for patients with pacemakers.
Published
2026-05-11
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
MR Unsafe
Rx
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
OZWIngestible Event Marker

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
OZWIngestible Event MarkerGeneral Hospital2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00857335005114PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00857335005114008573350051148573350051140857335005114

GMDN Terms#

Term, Definition table
TermDefinition
Gastrointestinal telemetric monitoring system capsule, ingestibleA battery-powered (conventional or physiologic), electronic component of a gastrointestinal telemetric monitoring system designed to be swallowed by a patient for the wireless signal transmission of one or more gastrointestinal parameters (i.e., pH, pressure, temperature) or events (e.g., gastrointestinal bleeding). The capsule contains a sensor(s) and the telemetric signals it produces are detected by an extracorporeal (e.g., patient-worn) receiver or transceiver; information is displayed by the receiver, or transmitted by the transceiver to a computer with software for display. The capsule is excreted from the gut. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Area/Surface Area32.1Square centimeter
Height6.9Millimeter
Length113.2Millimeter
Width45.2Millimeter

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Handling Environment Atmospheric Pressure70 KiloPascal106 KiloPascal
Handling Environment Humidity15 Percent (%) Relative Humidity93 Percent (%) Relative Humidity
Handling Environment Temperature5 Degrees Celsius40 Degrees Celsius
Storage Environment Humidity15 Percent (%) Relative Humidity93 Percent (%) Relative Humidity
Storage Environment Temperature5 Degrees Celsius27 Degrees Celsius

Contacts#

Phone, Email table
PhoneEmail
1.844.692.4834xx@xx.xx

Regulatory Flags#

DUNS number
008314390
Device count
1
Lot or batch
true
Serial number
true
Expiration date on label
true
Donation ID number
true

Other Devices From This Company#

Primary DI, Brand, Model table
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00857335005077Pediatric Urea Hydrolysis Rate Calculation Application pUHR-CA2.02017-04-19
00857335005039BreathTek® UBT for H. pylori Kit (Metabolic Solutions Kit)01M2017-05-16

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
10856602005236NAPROTEUS DIGITAL HEALTH, INC.OZW2019-07-12
10856602005243NAPROTEUS DIGITAL HEALTH, INC.OZW2019-07-12
10856602005250NAPROTEUS DIGITAL HEALTH, INC.OZW2019-07-12
10856602005267NAPROTEUS DIGITAL HEALTH, INC.OZW2019-07-12
10856602005274NAPROTEUS DIGITAL HEALTH, INC.OZW2019-07-12
20856602005172NAPROTEUS DIGITAL HEALTH, INC.OZW2019-07-12
10856602005144Proteus Digital Health Feedback SystemPROTEUS DIGITAL HEALTH, INC.OZW2018-07-02
00856602005130Proteus Digital Health Feedback SystemPROTEUS DIGITAL HEALTH, INC.OZW2018-07-02
10856602005137Proteus Digital Health Feedback SystemPROTEUS DIGITAL HEALTH, INC.OZW2018-07-02
00856602005215Proteus Digital Health Feedback SystemPROTEUS DIGITAL HEALTH, INC.OZW2018-07-02
00856602005222Proteus Digital Health Feedback SystemPROTEUS DIGITAL HEALTH, INC.OZW2018-07-02
10856602005168NAPROTEUS DIGITAL HEALTH, INC.OZW2018-05-18
10856602005175NAPROTEUS DIGITAL HEALTH, INC.OZW2018-05-18
10856602005182NAPROTEUS DIGITAL HEALTH, INC.OZW2018-05-18
10856602005199NAPROTEUS DIGITAL HEALTH, INC.OZW2018-05-18
10856602005205NAPROTEUS DIGITAL HEALTH, INC.OZW2018-05-18
00856602005154NAPROTEUS DIGITAL HEALTH, INC.OZW2017-05-08
10856602005083NAPROTEUS DIGITAL HEALTH, INC.OZW2016-09-22
10856602005090NAPROTEUS DIGITAL HEALTH, INC.OZW2016-09-22
10856602005106NAPROTEUS DIGITAL HEALTH, INC.OZW2016-09-22
10856602005113NAPROTEUS DIGITAL HEALTH, INC.OZW2016-09-22
10856602005120NAPROTEUS DIGITAL HEALTH, INC.OZW2016-09-22
00856602005017NAPROTEUS DIGITAL HEALTH, INC.OZW2016-07-07
10856602005021NAPROTEUS DIGITAL HEALTH, INC.OZW2016-07-07
10856602005045NAPROTEUS DIGITAL HEALTH, INC.OZW2016-07-07
10856602005052NAPROTEUS DIGITAL HEALTH, INC.OZW2016-07-07
10856602005069NAPROTEUS DIGITAL HEALTH, INC.OZW2016-07-07
10856602005076NAPROTEUS DIGITAL HEALTH, INC.OZW2016-07-07