Primary Device ID | M9703000112220200 |
NIH Device Record Key | e9a809ce-63c6-4ac4-a0ae-7a70c20c4fe6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DynaClip Quattro |
Version Model Number | 3000-11-222020 |
Company DUNS | 601306413 |
Company Name | Medshape, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | M9703000112220200 [Primary] |
JDR | Staple, Fixation, Bone |
Steralize Prior To Use | true |
Device Is Sterile | true |
[M9703000112220200]
Radiation Sterilization
[M9703000112220200]
Radiation Sterilization
[M9703000112220200]
Radiation Sterilization
[M9703000112220200]
Radiation Sterilization
[M9703000112220200]
Radiation Sterilization
[M9703000112220200]
Radiation Sterilization
[M9703000112220200]
Radiation Sterilization
[M9703000112220200]
Radiation Sterilization
[M9703000112220200]
Radiation Sterilization
[M9703000112220200]
Radiation Sterilization
[M9703000112220200]
Radiation Sterilization
[M9703000112220200]
Radiation Sterilization
[M9703000112220200]
Radiation Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2025-08-12 |
Device Publish Date | 2022-09-16 |
M9703000130000 | Procedure Pack, Dynaclip Quattro |
M9703000112220200 | QUATTRO DYNACLIP STAPLE, 22X20X20 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() DYNACLIP QUATTRO 97410229 not registered Live/Pending |
MedShape, Inc. 2022-05-13 |