Primary Device ID | 00840420121707 |
NIH Device Record Key | 0b243262-28ad-40c8-ab44-916d1c5a66f3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SWANSON |
Version Model Number | 4700020 |
Company DUNS | 807201207 |
Company Name | WRIGHT MEDICAL TECHNOLOGY, INC. |
Device Count | 1 |
DM Exempt | false |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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)238-7117 |
customerservice@wmt.com |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840420121707 [Primary] |
KWF | PROSTHESIS, FINGER, POLYMER |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-10-07 |
Device Publish Date | 2015-10-15 |