Duns Number:079881212
Device Description: ZIMMER® TRABECULAR METALTM REVERSE SHOULDER SYSTEM INSTRUMENTATION TECOMET REAMER 1 BLADE ZIMMER® TRABECULAR METALTM REVERSE SHOULDER SYSTEM INSTRUMENTATION TECOMET REAMER 1 BLADE - BOX OF 10
Catalog Number
11-167-511
Brand Name
ZIMMER® TRABECULAR METALTM REVERSE SHOULDER SYSTEM INSTRUMENTATION
Version/Model Number
47-4361-085-00
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"
-
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
-
Product Code
HWE
Product Code Name
Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
Public Device Record Key
3457f0f0-1a41-42b7-a58e-9e1080857718
Public Version Date
July 23, 2020
Public Version Number
3
DI Record Publish Date
June 18, 2019
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 201 |
2 | A medical device with a moderate to high risk that requires special controls. | 35 |