Primary Device ID | 10790986006383 |
NIH Device Record Key | 93ae6cbd-6c96-4940-b97a-7abde6255d2e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PDO |
Version Model Number | M303 |
Catalog Number | M303 |
Company DUNS | 807404611 |
Company Name | C.P. MEDICAL CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10790986006383 [Primary] |
NEW | Suture, Surgical, Absorbable, Polydioxanone |
Steralize Prior To Use | true |
Device Is Sterile | true |
[10790986006383]
Ethylene Oxide
[10790986006383]
Ethylene Oxide
[10790986006383]
Ethylene Oxide
[10790986006383]
Ethylene Oxide
[10790986006383]
Ethylene Oxide
[10790986006383]
Ethylene Oxide
[10790986006383]
Ethylene Oxide
[10790986006383]
Ethylene Oxide
[10790986006383]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2021-02-05 |
Device Publish Date | 2016-02-23 |
10790986006390 | M463 |
10790986006383 | M303 |