Duns Number:008124539
Device Description: Specimen Container- 4oz., Sterile, Individually Wrapped, Screw-On Leak-Resistant Lid, Tamp Specimen Container- 4oz., Sterile, Individually Wrapped, Screw-On Leak-Resistant Lid, Tamper-Evident Seal
Catalog Number
-
Brand Name
Specimen Container- 4oz., Sterile
Version/Model Number
4253
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
Yes
For Single-Use
Yes
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
FMH
Product Code Name
Container, Specimen, Sterile
Public Device Record Key
78c54cc7-6d9a-4d4c-9ad3-f1218d2032e1
Public Version Date
June 29, 2021
Public Version Number
1
DI Record Publish Date
June 21, 2021
Package DI Number
00616784425337
Quantity per Package
100
Contains DI Package
00616784425313
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Case
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 694 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 226 |
| 3 | A medical device with high risk that requires premarket approval | 2 |