Primary Device ID | 07613389772937 |
NIH Device Record Key | d0db16f4-c934-4912-92f0-3bee2ee504b7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MEMINI I 3 5P CIC-10 NWL PH |
Version Model Number | 10 NWL PH |
Catalog Number | 063-0532-01B1 |
Company DUNS | 480662550 |
Company Name | Sonova AG |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613389772937 [Primary] |
KLW | Masker, Tinnitus |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-20 |
Device Publish Date | 2024-11-12 |
07613389808070 - Phonak Audéo I-R Trial | 2025-01-16 |
07613389808087 - Phonak Audéo I-R Trial | 2025-01-16 |
07613389808094 - Phonak Audéo I-R Trial | 2025-01-16 |
07613389808100 - Phonak Audéo I-R Trial | 2025-01-16 |
07613389808117 - Phonak Audéo ISphereTrial | 2025-01-16 |
07613389808124 - Phonak Audéo ISphereTrial | 2025-01-16 |
07613389808131 - Phonak Audéo ISphereTrial | 2025-01-16 |
07613389808148 - Phonak Audéo ISphereTrial | 2025-01-16 |