Primary Device ID | M944FL4053110 |
NIH Device Record Key | 81b2e0bf-f74f-4b80-8119-d5230b3e61f6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Wexler Surgical, Inc. |
Version Model Number | FL4053.11 |
Company DUNS | 024882552 |
Company Name | WEXLER SURGICAL, 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 | 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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840240920603 [Secondary] |
HIBCC | M944FL4053110 [Primary] |
HTD | Forceps |
Steralize Prior To Use | true |
Device Is Sterile | false |
[M944FL4053110]
Moist Heat or Steam Sterilization
[M944FL4053110]
Moist Heat or Steam Sterilization
[M944FL4053110]
Moist Heat or Steam Sterilization
[M944FL4053110]
Moist Heat or Steam Sterilization
[M944FL4053110]
Moist Heat or Steam Sterilization
[M944FL4053110]
Moist Heat or Steam Sterilization
[M944FL4053110]
Moist Heat or Steam Sterilization
[M944FL4053110]
Moist Heat or Steam Sterilization
[M944FL4053110]
Moist Heat or Steam Sterilization
[M944FL4053110]
Moist Heat or Steam Sterilization
[M944FL4053110]
Moist Heat or Steam Sterilization
[M944FL4053110]
Moist Heat or Steam Sterilization
[M944FL4053110]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2021-12-02 |
Device Publish Date | 2017-11-22 |