Primary Device ID | 00735000695003 |
NIH Device Record Key | 4cb1fc28-adbb-47c4-b937-cf42a2a1ddf0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sonesta |
Version Model Number | S3 |
Company DUNS | 355118308 |
Company Name | Sonesta Medical AB |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Safe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
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 | 00735000695003 [Primary] |
MMZ | Table, Cystometric, Electric |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2017-03-28 |
00735000695003 | S3 |
07350006950025 | S2 |
07350006950018 | 6210 |
07350006950032 | S3 |
07350006950056 | SST |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SONESTA 97107081 not registered Live/Pending |
SONESTA TOOLS LLC 2021-11-03 |
SONESTA 88381052 not registered Live/Pending |
Ranco Industries, Inc. 2019-04-11 |
SONESTA 85543456 4303999 Dead/Cancelled |
Stille AB 2012-02-15 |
SONESTA 80992086 0992086 Dead/Cancelled |
Sonesta Internation Hotels Corporation 0000-00-00 |
SONESTA 77685686 3685842 Live/Registered |
SONESTA INTERNATIONAL HOTELS CORPORATION 2009-03-06 |
SONESTA 72333337 0897516 Dead/Cancelled |
HOTEL CORPORATION OF AMERICA 1969-07-24 |