Primary Device ID | 30884527004939 |
NIH Device Record Key | 3e8ee85c-fee6-4b4e-8e47-a80f6dac456f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Precision |
Version Model Number | 2210SA |
Catalog Number | 2210SA |
Company DUNS | 080935429 |
Company Name | Cardinal Health, Inc. |
Device Count | 100 |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com |
Height | 1.75 Inch |
Width | 1.75 Inch |
Total Volume | 1.5 Fluid Ounce |
Height | 1.75 Inch |
Width | 1.75 Inch |
Total Volume | 1.5 Fluid Ounce |
Height | 1.75 Inch |
Width | 1.75 Inch |
Total Volume | 1.5 Fluid Ounce |
Height | 1.75 Inch |
Width | 1.75 Inch |
Total Volume | 1.5 Fluid Ounce |
Height | 1.75 Inch |
Width | 1.75 Inch |
Total Volume | 1.5 Fluid Ounce |
Height | 1.75 Inch |
Width | 1.75 Inch |
Total Volume | 1.5 Fluid Ounce |
Height | 1.75 Inch |
Width | 1.75 Inch |
Total Volume | 1.5 Fluid Ounce |
Height | 1.75 Inch |
Width | 1.75 Inch |
Total Volume | 1.5 Fluid Ounce |
Height | 1.75 Inch |
Width | 1.75 Inch |
Total Volume | 1.5 Fluid Ounce |
Height | 1.75 Inch |
Width | 1.75 Inch |
Total Volume | 1.5 Fluid Ounce |
Height | 1.75 Inch |
Width | 1.75 Inch |
Total Volume | 1.5 Fluid Ounce |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry;AVOID DIRECT SUNLIGHT |
Device Issuing Agency | Device ID |
---|---|
GS1 | 20884527004932 [Primary] |
GS1 | 30884527004939 [Package] Contains: 20884527004932 Package: CASE [200 Units] In Commercial Distribution |
GS1 | 40884527004936 [Unit of Use] |
FMH | CONTAINER, SPECIMEN, STERILE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-02-15 |
Device Publish Date | 2018-06-29 |
10884527006823 | Catheter Urine Specimen System Kit |
20884527006813 | Stool Collector |
10884527006083 | Specimen Container,Positive Seal Indicator, OR Packaged |
10884527006052 | Specimen Container,Plastic Screw Top Cap, OR Packaged |
10884527006007 | Specimen Container,Plastic Screw Top Cap |
10884527005987 | Specimen Container,Metal Screw Top Cap, ID Label |
30884527004939 | Specimen Container,Positive Seal Indicator |
40884527005957 | Urine Specimen System with Preservative |
20884527006103 | Midstream Preservative Kit |
20884527004895 | Tissue Grinder |
20884527004888 | Tissue Grinder |
20884527006448 | Sputum Collector Kit with Tube |
10884527004928 | Specimen Container,Positive Seal Indicator |
20884527006806 | Specimen Container,Positive Seal Indicator |
10884527004607 | Specimen Container,Positive Seal Indicator |
10884527004584 | Specimen Container,No Cap |