Primary Device ID | M543CM6202 |
NIH Device Record Key | 927d4ba0-6c35-407b-bfb1-8a0ebbcdbe28 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BioWick X® |
Version Model Number | CM-6202 |
Catalog Number | CM-6202 |
Company DUNS | 606719685 |
Company Name | CAYENNE MEDICAL, 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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | M543CM6202 [Primary] |
HWX | Tap, Bone |
Steralize Prior To Use | true |
Device Is Sterile | false |
[M543CM6202]
Moist Heat or Steam Sterilization
[M543CM6202]
Moist Heat or Steam Sterilization
[M543CM6202]
Moist Heat or Steam Sterilization
[M543CM6202]
Moist Heat or Steam Sterilization
[M543CM6202]
Moist Heat or Steam Sterilization
[M543CM6202]
Moist Heat or Steam Sterilization
[M543CM6202]
Moist Heat or Steam Sterilization
[M543CM6202]
Moist Heat or Steam Sterilization
[M543CM6202]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-04-08 |
Device Publish Date | 2019-03-29 |
M543CM6202 | CM-6202 |
M543CM6201 | CM-6201 |
00887868269783 | CM-6202 |
00887868269776 | CM-6201 |