Primary Device ID | M944AL2040120 |
NIH Device Record Key | 8b0ae87a-3758-4cd9-ba44-dcb272df1053 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Wexler Surgical, Inc. |
Version Model Number | AL2040.12 |
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 | 00840240936888 [Secondary] |
HIBCC | M944AL2040120 [Primary] |
HTD | Forceps |
Steralize Prior To Use | true |
Device Is Sterile | false |
[M944AL2040120]
Moist Heat or Steam Sterilization
[M944AL2040120]
Moist Heat or Steam Sterilization
[M944AL2040120]
Moist Heat or Steam Sterilization
[M944AL2040120]
Moist Heat or Steam Sterilization
[M944AL2040120]
Moist Heat or Steam Sterilization
[M944AL2040120]
Moist Heat or Steam Sterilization
[M944AL2040120]
Moist Heat or Steam Sterilization
[M944AL2040120]
Moist Heat or Steam Sterilization
[M944AL2040120]
Moist Heat or Steam Sterilization
[M944AL2040120]
Moist Heat or Steam Sterilization
[M944AL2040120]
Moist Heat or Steam Sterilization
[M944AL2040120]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2022-03-21 |
Device Publish Date | 2022-02-28 |