Primary Device ID | 20845854043780 |
NIH Device Record Key | 6b351705-e770-4470-be32-74d69d55e781 |
Commercial Distribution Discontinuation | 2021-02-11 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Tenolok |
Version Model Number | T50S |
Catalog Number | T50S |
Company DUNS | 071595540 |
Company Name | Conmed Corporation |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
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 |
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 | |
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 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
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 |
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 | 20845854043780 [Primary] |
MBI | Fastener, fixation, nondegradable, soft tissue |
Steralize Prior To Use | true |
Device Is Sterile | true |
[20845854043780]
Ethylene Oxide
[20845854043780]
Ethylene Oxide
[20845854043780]
Ethylene Oxide
[20845854043780]
Ethylene Oxide
[20845854043780]
Ethylene Oxide
[20845854043780]
Ethylene Oxide
[20845854043780]
Ethylene Oxide
[20845854043780]
Ethylene Oxide
[20845854043780]
Ethylene Oxide
[20845854043780]
Ethylene Oxide
[20845854043780]
Ethylene Oxide
[20845854043780]
Ethylene Oxide
[20845854043780]
Ethylene Oxide
[20845854043780]
Ethylene Oxide
[20845854043780]
Ethylene Oxide
[20845854043780]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2021-02-11 |
Device Publish Date | 2020-11-12 |
10845854044711 | T60A80 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor with One No. 2 Hi-Fi Suture, 2.4 mm Guid |
10845854044704 | T60S80 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor, 2.4 mm Guide Pin, and 8.0 mm Drill Bit |
10845854044681 | T60A75 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor with One No. 2 Hi-Fi Suture, 2.4 mm Guid |
10845854044667 | T50S65 TenoLok Tenodesis Kit with 5.0 mm TenoLok Anchor with One No. 2 Hi-Fi Suture, 2.4 mm Guid |
20845854044671 | Tenolok Tenodesis Kit With 5.0mm Tenolok Anchor with One #2 Hi-Fi Suture, 2.4mm Guide Pin, And 7 |
20845854043780 | 5.0 mm Tenolok Tenodesis Anchor with one No. 2 Hi-Fi Suture |
20653405987182 | T60A75 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor with One No. 2 Hi-Fi Suture, 2.4 mm Guid |
20653405987175 | T60A80 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor with One No. 2 Hi-Fi Suture, 2.4 mm Guid |
20653405987168 | T50S65 TenoLok Tenodesis Kit with 5.0 mm TenoLok Anchor with One No. 2 Hi-Fi Suture, 2.4 mm Guid |
20653405987151 | T60S80 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor, 2.4 mm Guide Pin, and 8.0 mm Drill Bit |
10845854044698 | T60S75 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor, 2.4 mm Guide Pin, and 7.5 mm Drill Bit |
30845854044678 | Tenolok Tenodesis Kit With 5.0mm Tenolok Anchor with One #2 Hi-Fi Suture, 2.4mm Guide Pin, And 7 |
30845854043787 | 5.0 mm Tenolok Tenodesis Anchor with one No. 2 Hi-Fi Suture |
20653405987199 | T60S75 TenoLok Tenodesis Kit with 6.0 mm TenoLok Anchor, 2.4 mm Guide Pin, and 7.5 mm Drill Bit |
10845854043806 | TenoLok 6.0mm Tenodesis Anchor |
10845854043790 | TenoLok 6.0 mm Tenodesis Anchor with One #2 Hi-Fi Suture |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TENOLOK 86719830 4948048 Live/Registered |
Conmed Corporation 2015-08-10 |