| Primary Device ID | M944FL0203110 |
| NIH Device Record Key | 104e13bc-a62d-4b53-ae7a-a73e6bfe4a6a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Wexler Surgical, Inc. |
| Version Model Number | FL0203.11 |
| 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 | 00840240915869 [Secondary] |
| HIBCC | M944FL0203110 [Primary] |
| HNR | Forceps, Ophthalmic |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[M944FL0203110]
Moist Heat or Steam Sterilization
[M944FL0203110]
Moist Heat or Steam Sterilization
[M944FL0203110]
Moist Heat or Steam Sterilization
[M944FL0203110]
Moist Heat or Steam Sterilization
[M944FL0203110]
Moist Heat or Steam Sterilization
[M944FL0203110]
Moist Heat or Steam Sterilization
[M944FL0203110]
Moist Heat or Steam Sterilization
[M944FL0203110]
Moist Heat or Steam Sterilization
[M944FL0203110]
Moist Heat or Steam Sterilization
[M944FL0203110]
Moist Heat or Steam Sterilization
[M944FL0203110]
Moist Heat or Steam Sterilization
[M944FL0203110]
Moist Heat or Steam Sterilization
[M944FL0203110]
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 | 2017-11-20 |