Primary Device ID | 00885556533277 |
NIH Device Record Key | 31c9cec3-8045-4e37-9cdf-e325452c622c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ACUFEX Meniscal Root Repair |
Version Model Number | 71935068 |
Catalog Number | 71935068 |
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 | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
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 |
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Phone | +1(800)238-7538 |
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Phone | +1(800)238-7538 |
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Phone | +1(800)238-7538 |
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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 | 00885556533277 [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 | 2020-02-06 |
Device Publish Date | 2016-12-19 |
00885556624760 | MENISCAL ROOT REPAIR INSTRUMENTS PACK |
00885556533291 | MENISCAL ROOT REPAIR PACK WITH ULTRABRAID¿ |
00885556533277 | MENISCAL ROOT REPAIR PACK WITH ULTRATAPE |