Vacuflow™ MED 5023
GUDID 20850011007055
Butterfly, Vacuflow non-safety, w/adapter 23G 12" tubing 50/bx
MERCEDES MEDICAL, LLC
Venous butterfly needle/set| Primary Device ID | 20850011007055 |
| NIH Device Record Key | 2a0835ae-5b4c-4be0-97fc-0496265ba544 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Vacuflow™ |
| Version Model Number | MED 5023 |
| Catalog Number | MED 5023 |
| Company DUNS | 834472680 |
| Company Name | MERCEDES MEDICAL, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | true |
| 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 |
Customer Support Contacts
| Phone | 800-331-2716 |
| sherry.harris@mercedesmedical.com | |
| Phone | 800-331-2716 |
| sherry.harris@mercedesmedical.com | |
| Phone | 800-331-2716 |
| sherry.harris@mercedesmedical.com | |
| Phone | 800-331-2716 |
| sherry.harris@mercedesmedical.com | |
| Phone | 800-331-2716 |
| sherry.harris@mercedesmedical.com | |
| Phone | 800-331-2716 |
| sherry.harris@mercedesmedical.com | |
| Phone | 800-331-2716 |
| sherry.harris@mercedesmedical.com | |
| Phone | 800-331-2716 |
| sherry.harris@mercedesmedical.com | |
| Phone | 800-331-2716 |
| sherry.harris@mercedesmedical.com | |
| Phone | 800-331-2716 |
| sherry.harris@mercedesmedical.com | |
| Phone | 800-331-2716 |
| sherry.harris@mercedesmedical.com | |
| Phone | 800-331-2716 |
| sherry.harris@mercedesmedical.com | |
| Phone | 800-331-2716 |
| sherry.harris@mercedesmedical.com | |
| Phone | 800-331-2716 |
| sherry.harris@mercedesmedical.com | |
| Phone | 800-331-2716 |
| sherry.harris@mercedesmedical.com |
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850011007051 [Primary] |
| GS1 | 10850011007058 [Package] Contains: 00850011007051 Package: Inner Pack [50 Units] In Commercial Distribution |
| GS1 | 20850011007055 [Package] Contains: 10850011007058 Package: Case [4 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K000714
FDA Product Code
| JKA | Tubes, Vials, Systems, Serum Separators, Blood Collection |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-10-23 |
| Device Publish Date | 2016-08-15 |
On-Brand Devices [Vacuflow™]
| 00850011007211 | Butterfly Safety Luer Adapter 25g; 50bx |
| 20850011007208 | Vacuflow Butterfly Safety Luer Adapter 23g; 50bx |
| 00850011007198 | Vacuflow Butterfly Safety Luer Adapter 21g; 50bx |
| 00850011007181 | Butterfly, Vacuflow non-safety, w/adapter 25G 12" tubing 50/bx |
| 20850011007055 | Butterfly, Vacuflow non-safety, w/adapter 23G 12" tubing 50/bx |
| 00850011007006 | Butterfly, Vacuflow non-safety, w/adapter 21G 12" tubing 50/bx |
Trademark Results [Vacuflow]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 VACUFLOW 86249772 4689990 Live/Registered |
MERCEDES MEDICAL, LLC 2014-04-11 |
 VACUFLOW 73240797 1152932 Dead/Cancelled |
Pneumatic Scale Corporation 1979-11-29 |
 VACUFLOW 71663945 0610622 Dead/Expired |
PNEUMATIC SCALE CORPORATION, LIMITED 1954-04-05 |
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