Primary Device ID | D928105530R0 |
NIH Device Record Key | fe25b572-bb7e-4e5c-beb8-3caa25878b68 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RETRACTOR U OF MINNESOTA REVERSE BEND |
Version Model Number | 10-5530R |
Company DUNS | 183854322 |
Company Name | W.H. Holden, 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 | true |
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 |
---|---|
HIBCC | D928105530R0 [Primary] |
GAD | Retractor |
Steralize Prior To Use | true |
Device Is Sterile | false |
[D928105530R0]
Moist Heat or Steam Sterilization
[D928105530R0]
Moist Heat or Steam Sterilization
[D928105530R0]
Moist Heat or Steam Sterilization
[D928105530R0]
Moist Heat or Steam Sterilization
[D928105530R0]
Moist Heat or Steam Sterilization
[D928105530R0]
Moist Heat or Steam Sterilization
[D928105530R0]
Moist Heat or Steam Sterilization
[D928105530R0]
Moist Heat or Steam Sterilization
[D928105530R0]
Moist Heat or Steam Sterilization
[D928105530R0]
Moist Heat or Steam Sterilization
[D928105530R0]
Moist Heat or Steam Sterilization
[D928105530R0]
Moist Heat or Steam Sterilization
[D928105530R0]
Moist Heat or Steam Sterilization
[D928105530R0]
Moist Heat or Steam Sterilization
[D928105530R0]
Moist Heat or Steam Sterilization
[D928105530R0]
Moist Heat or Steam Sterilization
[D928105530R0]
Moist Heat or Steam Sterilization
[D928105530R0]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-26 |
Device Publish Date | 2024-12-18 |