Home GUDID 05075020066416
Philips health watch
Primary DI 05075020066416
Brand Philips health watch
Company Philips Medical Systems Nederland B.V.
Model DL8791
Device description retail version
Published 2016-09-17
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx false
OTC true
Sterile false
Single use false Product Codes# Code, Name table Code Name ISD Exerciser, Measuring
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class ISD Exerciser, Measuring Physical Medicine 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 05075020066416 Package GS1 9 In Commercial Distribution 10075020008449 Package GS1 2 In Commercial Distribution 20075020057079 Package GS1 4 In Commercial Distribution 00075020058157 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 05075020066416 05075020066416 5075020066416 10075020008449 10075020008449 20075020057079 20075020057079 00075020058157 00075020058157 075020058157 0075020058157
GMDN Terms# Term, Definition table Term Definition Photoplethysmography/accelerometery recording sensor An electrically-powered, wearable device (e.g., wristband, finger probe, head-worn sensor) designed to continuously measure and record: 1) photoplethysmography (PPG) data (e.g., pertaining to heart rate, respiration rate); and, 2) movement, during normal day- and/or night-time activities at home. It includes an optical PPG sensor and an accelerometer. The data is typically transferred to a local application or central database for analysis which includes evaluation of lifestyle factors (e.g., energy expenditure, activity level, sleep patterns).
Regulatory Flags# DUNS number 489844773 Device count 1 DM exempt false Premarket exempt true HCT/P false Kit false Combination product false Lot or batch false Serial number true Manufacturing date on label false Expiration date on label false Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00884838123786 Multimodality Simulation Workspace (MM Sim)1.0 Multimodality Simulation Workspace (MM Sim)1.0 728349 2026-06-07 00884838123793 Multimodality Simulation Workspace (MM Sim)1.0 Upgrade Multimodality Simulation Workspace (MM Sim)1.0 Upg 728351 2026-06-07 00884838123748 Spectral CT Verida Spectral CT Verida 728345 2026-05-26 00884838126398 Spectral CT Verida RT Spectral CT Verida RT 728357 2026-05-26 00884838127555 Upgrade Spectral CT Verida Upgrade Spectral CT Verida 728356 2026-05-26 00884838127562 Upgrade Spectral CT Verida RT Upgrade Spectral CT Verida RT 728372 2026-05-26 00884838127876 Upgrade Spectral CT 7500 SW5.4 Upgrade Spectral CT 7500 SW5.4 728375 2026-05-26 00884838127883 Upgrades Spectral CT 7500 RT SW5.4 Upgrades Spectral CT 7500 RT SW5.4 728355 2026-05-26 00884838128187 Ingenia BlueSeal SE 782213 2026-04-07 00884838128194 Ingenia BlueSeal XE 782214 2026-04-07 00884838128200 Ingenia Ingenia Elition S 782216 2026-04-07 00884838128217 Ingenia Ingenia Elition X 782217 2026-04-07 00884838128224 MR 7700 MR 7700 782218 2026-04-07 00884838128231 Ingenia Upgrades dStream to R13 782219 2026-04-07 00884838128248 Ingenia Evolution Upgrade 1.5T 782220 2026-04-07 00884838128255 Ingenia Evolution Upgrade 3.0T 782221 2026-04-07 00884838128262 Ingenia SmartPath to Ingenia Elition X 782222 2026-04-07 00884838128293 MR 7700 Upgrade to MR 7700 782225 2026-04-07 00884838128309 MR 7700 SmartPath to MR 7700 782226 2026-04-07 00884838128316 Ingenia BlueSeal QE 782215 2026-04-07
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