Primary Device ID | 03596010498496 |
NIH Device Record Key | 380be56c-545e-46b2-b641-f9cf4bca3bb3 |
Commercial Distribution Discontinuation | 2020-05-31 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | TWINFIX / DURABRAID |
Version Model Number | 7210210 |
Catalog Number | 7210210 |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03596010498496 [Primary] |
MAI | FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2020-06-02 |
Device Publish Date | 2016-04-12 |
03596010585974 | TWINFIX AB 6.5 SUTR ANCR W/2 DURABRAID |
03596010584489 | TWINFIX TI 2.8 HS SUTR ANCHR W/2 28 DUR |
03596010498502 | TWNFX AB 6.5 STR ANCHR2 38 DRBRD STR ND |
03596010485656 | TWINFIX TI 5.0 SUTURE ANCHOR W/TWO 38 |
03596010498496 | TWNFX AB 6.5 STR ANCHR 2 38 DB STR |
03596010001238 | TWNFIX AB 6.5 STR ANCHR 2 DRBRD 38 |
03596010495440 | TWNFX TI 6.5 SUTURE ANCHOR WITH TWO 38 |
03596010533838 | TWINFXTI2.8 STR ANCHR W/DURBRD STR 2-0 |