AccessGUDID - DEVICE: Sentiero Advanced (04260223145247)

GUDID

Device Identifier (DI) Information

Brand Name: Sentiero Advanced
Version or Model: 100340-SC-ALL-LT
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: PATH medical GmbH

Primary DI Number: 04260223145247
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 551540334 *Terms of Use

Device Description: Sentiero Advanced ABR, OAE, Tympanometry and Audio Screening Set Content: 1. Case AN100503 2. Inlay Sentiero AN100677 3. USB data cable AN100089 4. Path electrodes: 30 pcs. / bag. Each bag contains 10 sets of 3 pcs. AN 100468 5. Sentiero Advanced device with touchscreen AN100360 6. ABR electrode cable AN100307 7. Headphone DD-45 AN100306 8. Probe EP-LT AN101021 9. Accessory box EP-LT AN101043 10. ABR Quick SW AN100337-Quick 11. TEOAE Quick SW AN100109-Quick 12. DPOAE Quick SW AN100110-Quick 13. FMDPOAE SW AN100536 14. Tymp Class 2 SW AN100560 15. Audio Class 4 Advanced SW AN100653 16. Mira PC Patient Management SW AN100116 17. Label Printer SW AN100414 18. Power Supply Sentiero Advanced US AN101016+AN100993-USA 19. Tympanometry add-on TY-MA AN100947 20. Accessory box AB08 AN100734-P 21. Tympanometry cavity AN100549 22. Probe tip small PT-S AN100014-W (3 pcs.) 23. Probe tip medium PT-A AN100013 (5 pcs.)

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	Yes
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
35747	Evoked-potential audiometer	An electroacoustic instrument designed to evaluate the activity of the auditory pathway of the brain in response to an acoustic signal [auditory brainstem response (ABR)] it provides at the ear (e.g., clicks delivered through an earphone), without need of patient cooperation. The signal, detected via the device's scalp electrodes and possibly a reference electrode on the ear lobe, is measured using computer averaging and signal processing techniques. This device is typically used to assess the function of the auditory pathways and to differentiate coma due to metabolic factors from structural damage.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GWJ	Stimulator, Auditory, Evoked Response
EWO	Audiometer
ETY	Tester, Auditory Impedance

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 1e17b35c-69a9-4b2d-ae09-34258877e675
Public Version Date: June 30, 2022
Public Version Number: 3
DI Record Publish Date: June 27, 2020