SafeGuide® Single 1215-30
GUDID 00816734023235
Disposable Over the Guidewire Esophageal Dilator, 30 FR
DIVERSATEK HEALTHCARE, INC.
Over-guidewire oesophageal dilator| Primary Device ID | 00816734023235 |
| NIH Device Record Key | 18083184-9d7b-49ed-a5ca-9feb22b6964a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SafeGuide® Single |
| Version Model Number | 1215-30 |
| Catalog Number | 1215-30 |
| Company DUNS | 030650113 |
| Company Name | DIVERSATEK HEALTHCARE, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | 800-558-6408 |
| sales@diversatekhc.com | |
| Phone | 800-558-6408 |
| sales@diversatekhc.com | |
| Phone | 800-558-6408 |
| sales@diversatekhc.com | |
| Phone | 800-558-6408 |
| sales@diversatekhc.com | |
| Phone | 800-558-6408 |
| sales@diversatekhc.com | |
| Phone | 800-558-6408 |
| sales@diversatekhc.com | |
| Phone | 800-558-6408 |
| sales@diversatekhc.com | |
| Phone | 800-558-6408 |
| sales@diversatekhc.com | |
| Phone | 800-558-6408 |
| sales@diversatekhc.com | |
| Phone | 800-558-6408 |
| sales@diversatekhc.com | |
| Phone | 800-558-6408 |
| sales@diversatekhc.com | |
| Phone | 800-558-6408 |
| sales@diversatekhc.com | |
| Phone | 800-558-6408 |
| sales@diversatekhc.com | |
| Phone | 800-558-6408 |
| sales@diversatekhc.com | |
| Phone | 800-558-6408 |
| sales@diversatekhc.com | |
| Phone | 800-558-6408 |
| sales@diversatekhc.com | |
| Phone | 800-558-6408 |
| sales@diversatekhc.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00816734023235 [Primary] |
FDA Product Code
| KNQ | Dilator, Esophageal |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-08-22 |
| Device Publish Date | 2023-08-14 |
On-Brand Devices [SafeGuide® Single]
| 00816734023334 | Disposable Over the Guidewire Esophageal Dilator, 60 FR |
| 00816734023327 | Disposable Over the Guidewire Esophageal Dilator, 57 FR |
| 00816734023310 | Disposable Over the Guidewire Esophageal Dilator, 54 FR |
| 00816734023303 | Disposable Over the Guidewire Esophageal Dilator, 51 FR |
| 00816734023297 | Disposable Over the Guidewire Esophageal Dilator, 48 FR |
| 00816734023280 | Disposable Over the Guidewire Esophageal Dilator, 45 FR |
| 00816734023273 | Disposable Over the Guidewire Esophageal Dilator, 42 FR |
| 00816734023266 | Disposable Over the Guidewire Esophageal Dilator, 39 FR |
| 00816734023259 | Disposable Over the Guidewire Esophageal Dilator, 36 FR |
| 00816734023242 | Disposable Over the Guidewire Esophageal Dilator, 33 FR |
| 00816734023235 | Disposable Over the Guidewire Esophageal Dilator, 30 FR |
| 00816734023228 | Disposable Over the Guidewire Esophageal Dilator, 27 FR |
| 00816734023211 | Disposable Over the Guidewire Esophageal Dilator, 24 FR |
| 00816734023204 | Disposable Over the Guidewire Esophageal Dilator, 21 FR |
| 00816734023198 | Disposable Over the Guidewire Esophageal Dilator, 18 FR |
| 00816734023181 | Disposable Over the Guidewire Esophageal Dilator, 15 FR |
Trademark Results [SafeGuide]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SAFEGUIDE 98742968 not registered Live/Pending |
DuPont Safety & Construction, Inc. 2024-09-10 |
 SAFEGUIDE 85881711 4550149 Live/Registered |
DIVERSATEK HEALTHCARE, INC. 2013-03-20 |
 SAFEGUIDE 72314405 0873527 Dead/Expired |
BECTON, DICKINSON AND COMPANY 1968-12-13 |
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