Primary Device ID | M791WF1000 |
NIH Device Record Key | a41e7227-5457-44f2-9e84-71fc87e6437c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Wire Fixation |
Version Model Number | WF100 |
Company DUNS | 942203001 |
Company Name | BIOACCESS 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 | false |
Expiration Date | true |
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 | M791WF1000 [Primary] |
GFF | Bur, Surgical, General & Plastic Surgery |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-08-12 |
Device Publish Date | 2022-08-04 |
M791NGD10000 - Next Gen Driver | 2022-08-12 |
M791NGD1005A0 - Next Gen Driver | 2022-08-12 |
M791SBT10000 - Small Bone Tool | 2022-08-12 |
M791SBT1000HT0 - Small Bone Tool | 2022-08-12 |
M791SBT10010 - Small Bone Tool | 2022-08-12 |
M791SBT1001A0 - Small Bone Tool | 2022-08-12 |
M791SBT10040 - Small Bone Tool | 2022-08-12 |
M791SBT10050 - Small Bone Tool | 2022-08-12 |