Primary Device ID | 03596010566140 |
NIH Device Record Key | 24a10b5b-b1f0-4220-aee2-cc53530600cd |
Commercial Distribution Discontinuation | 2020-10-23 |
Commercial Distribution Status | Not in Commercial Distribution |
Version Model Number | 7207951S |
Catalog Number | 7207951S |
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 | 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 | true |
OTC Over-The-Counter | false |
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 Issuing Agency | Device ID |
---|---|
GS1 | 03596010566140 [Primary] |
GCJ | Laparoscope, general & plastic surgery |
Steralize Prior To Use | true |
Device Is Sterile | false |
[03596010566140]
Moist Heat or Steam Sterilization
[03596010566140]
Moist Heat or Steam Sterilization
[03596010566140]
Moist Heat or Steam Sterilization
[03596010566140]
Moist Heat or Steam Sterilization
[03596010566140]
Moist Heat or Steam Sterilization
[03596010566140]
Moist Heat or Steam Sterilization
[03596010566140]
Moist Heat or Steam Sterilization
[03596010566140]
Moist Heat or Steam Sterilization
[03596010566140]
Moist Heat or Steam Sterilization
[03596010566140]
Moist Heat or Steam Sterilization
[03596010566140]
Moist Heat or Steam Sterilization
[03596010566140]
Moist Heat or Steam Sterilization
[03596010566140]
Moist Heat or Steam Sterilization
[03596010566140]
Moist Heat or Steam Sterilization
[03596010566140]
Moist Heat or Steam Sterilization
[03596010566140]
Moist Heat or Steam Sterilization
[03596010566140]
Moist Heat or Steam Sterilization
[03596010566140]
Moist Heat or Steam Sterilization
[03596010566140]
Moist Heat or Steam Sterilization
[03596010566140]
Moist Heat or Steam Sterilization
[03596010566140]
Moist Heat or Steam Sterilization
[03596010566140]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-10-26 |
Device Publish Date | 2015-09-28 |
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