Primary Device ID | 23596010587682 |
NIH Device Record Key | b7406384-2124-42fe-995e-7c8435e7698a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FOOTPRINT |
Version Model Number | 72200879 |
Catalog Number | 72200879 |
Company DUNS | 045483575 |
Company Name | Smith & Nephew, Inc. |
Device Count | 2 |
DM Exempt | true |
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 | false |
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 |
GUDID@SMITH-NEPHEW.COM | |
Phone | +1(800)238-7538 |
GUDID@SMITH-NEPHEW.COM |
Special Storage Condition, Specify | Between 0 and 0 *: - |
Special Storage Condition, Specify | Between 0 and 0 *: - |
Special Storage Condition, Specify | Between 0 and 0 *: - |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03596010587688 [Unit of Use] |
GS1 | 23596010587682 [Primary] |
NBH | ACCESSORIES,ARTHROSCOPIC |
Steralize Prior To Use | true |
Device Is Sterile | false |
[23596010587682]
Moist Heat or Steam Sterilization
[23596010587682]
Moist Heat or Steam Sterilization
[23596010587682]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2025-01-10 |
Device Publish Date | 2015-08-29 |
03596010650535 | FOOTPRINT ULTRA PK SUTURE ANCHOR 5.5 |
03596010650528 | FOOTPRINT ULTRA PK SUTURE ANCHOR 4.5 |
00885556901335 | FOOTPRINT MINI DRILL 3.7MM |
00885556890912 | FOOTPRINT MINI DRILL 3.5MM |
00885556890769 | FOOTPRINT MINI PK 3.5MM |
23596010587682 | REPLACEMENT END CAPS FOR MALLET SET OF 2 |