Primary Device ID | 00849554014800 |
NIH Device Record Key | 73e7aa16-df33-4ea3-a4fb-8c2c73602c5f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 3M™ V.A.C. |
Version Model Number | ULTVCC05MD |
Catalog Number | ULTVCC05MD |
Company DUNS | 102726734 |
Company Name | KCI USA, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)228-3957 |
3Mhealthcarecompliance@mmm.com | |
Phone | +1(800)228-3957 |
3Mhealthcarecompliance@mmm.com | |
Phone | +1(800)228-3957 |
3Mhealthcarecompliance@mmm.com | |
Phone | +1(800)228-3957 |
3Mhealthcarecompliance@mmm.com | |
Phone | +1(800)228-3957 |
3Mhealthcarecompliance@mmm.com | |
Phone | +1(800)228-3957 |
3Mhealthcarecompliance@mmm.com | |
Phone | +1(800)228-3957 |
3Mhealthcarecompliance@mmm.com | |
Phone | +1(800)228-3957 |
3Mhealthcarecompliance@mmm.com | |
Phone | +1(800)228-3957 |
3Mhealthcarecompliance@mmm.com | |
Phone | +1(800)228-3957 |
3Mhealthcarecompliance@mmm.com | |
Phone | +1(800)228-3957 |
3Mhealthcarecompliance@mmm.com | |
Phone | +1(800)228-3957 |
3Mhealthcarecompliance@mmm.com | |
Phone | +1(800)228-3957 |
3Mhealthcarecompliance@mmm.com | |
Phone | +1(800)228-3957 |
3Mhealthcarecompliance@mmm.com | |
Phone | +1(800)228-3957 |
3Mhealthcarecompliance@mmm.com | |
Phone | +1(800)228-3957 |
3Mhealthcarecompliance@mmm.com | |
Phone | +1(800)228-3957 |
3Mhealthcarecompliance@mmm.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00849554014060 [Primary] |
GS1 | 00849554014800 [Package] Contains: 00849554014060 Package: [5 Units] In Commercial Distribution |
OMP | negative pressure wound therapy Powered suction pump |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-05-23 |
Device Publish Date | 2024-05-15 |
00849554014817 | Veraflo Cleanse Choice™ Dressing, ULTVCC05LG, Large, Cavilon Warning Label, 5/CS |
00849554014800 | Veraflo Cleanse Choice™ Dressing, ULTVCC05MD, Medium, Cavilon Warning Label, 5/CS |