Primary Device ID | 10845854042243 |
NIH Device Record Key | 23e9b58d-e26e-4a68-b280-5dc2f5cd92dc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SPECTRUM AUTOPASS |
Version Model Number | SMI-02AP |
Catalog Number | SMI-02AP |
Company DUNS | 071595540 |
Company Name | Conmed Corporation |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com | |
Phone | +1(866)426-6633 |
CustomerExperience@conmed.com |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10845854042243 [Primary] |
GS1 | 20845854042240 [Direct Marking] |
LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2022-07-25 |
Device Publish Date | 2021-05-30 |
10845854042243 | SPECTRUM AUTOPASS SUTURE PASSER |
20845854045753 | SPECTRUM AUTOPASS SUTURE PASSER NEEDLE |