Duns Number:080458964
Device Description: Sterile Equipment Drape, Tetra Mobile X-Ray Image Intensifier
Catalog Number
956925TET
Brand Name
Spectrum, Inc.
Version/Model Number
982-03725-000
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Safe
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K934630,K934630,K934630
Product Code
LPZ
Product Code Name
Container, frozen donor tissue storage
Public Device Record Key
a729fdcf-6df9-482e-a73c-80fbef2a0f8a
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
July 21, 2017
Package DI Number
20855495007324
Quantity per Package
20
Contains DI Package
10855495007327
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Shipper
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 66 |
2 | A medical device with a moderate to high risk that requires special controls. | 16 |
U | Unclassified | 11 |