VERSITIP 2146
GUDID 03596010103345
DYONICS/WOLF INSTR VERSITIP
Smith & Nephew, Inc.
Endoscopic light source adaptor| Primary Device ID | 03596010103345 |
| NIH Device Record Key | c65bd3f8-d1f1-4d3c-a35a-83bf92a8b205 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VERSITIP |
| Version Model Number | 2146 |
| Catalog Number | 2146 |
| Company DUNS | 109903521 |
| Company Name | Smith & Nephew, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| 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 | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | +1(800)821-5700 |
| gudid@smith-nephew.com | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM | |
| Phone | +1(800)238-7538 |
| GUDID@SMITH-NEPHEW.COM |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03596010103345 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K914919
FDA Product Code
| GCJ | Laparoscope, general & plastic surgery |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
[03596010103345]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-01-31 |
| Device Publish Date | 2015-08-30 |
On-Brand Devices [VERSITIP]
| 03596010103352 | DYONICS/WOLF SOURCE VERSITIP |
| 03596010103345 | DYONICS/WOLF INSTR VERSITIP |
| 03596010103338 | VERSITIP OLY SOURCE |
| 03596010103321 | VERSITIP STO SOURCE |
| 03596010103314 | VERSITIP STO/OLY INS |
| 03596010103307 | VERSITIP ACMI SOURCE |
| 03596010103291 | VERSITIP ACMI INS 4 & 5MM L/G |
Trademark Results [VERSITIP]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 VERSITIP 75030310 2015607 Live/Registered |
RIO PRODUCTS INTL., INC. 1995-12-06 |
VERSITIP 75030310 2015607 Live/Registered |
Vincent, Cecily C Pearson 1995-12-06 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.