Primary Device ID | 20845854037642 |
NIH Device Record Key | 48fa38df-368c-4290-9c50-7d1132ba4f5c |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 2.7009 |
Catalog Number | 2.7009 |
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 | false |
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 | |
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 |
Width | 2.75 Millimeter |
Length | 90 Millimeter |
Width | 2.75 Millimeter |
Length | 90 Millimeter |
Width | 2.75 Millimeter |
Length | 90 Millimeter |
Width | 2.75 Millimeter |
Length | 90 Millimeter |
Width | 2.75 Millimeter |
Length | 90 Millimeter |
Width | 2.75 Millimeter |
Length | 90 Millimeter |
Width | 2.75 Millimeter |
Length | 90 Millimeter |
Width | 2.75 Millimeter |
Length | 90 Millimeter |
Width | 2.75 Millimeter |
Length | 90 Millimeter |
Width | 2.75 Millimeter |
Length | 90 Millimeter |
Width | 2.75 Millimeter |
Length | 90 Millimeter |
Width | 2.75 Millimeter |
Length | 90 Millimeter |
Width | 2.75 Millimeter |
Length | 90 Millimeter |
Width | 2.75 Millimeter |
Length | 90 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10845854037645 [Primary] |
GS1 | 20845854037642 [Direct Marking] |
GEN | FORCEPS, GENERAL & PLASTIC SURGERY |
Steralize Prior To Use | true |
Device Is Sterile | false |
[20845854037642]
Moist Heat or Steam Sterilization
[20845854037642]
Moist Heat or Steam Sterilization
[20845854037642]
Moist Heat or Steam Sterilization
[20845854037642]
Moist Heat or Steam Sterilization
[20845854037642]
Moist Heat or Steam Sterilization
[20845854037642]
Moist Heat or Steam Sterilization
[20845854037642]
Moist Heat or Steam Sterilization
[20845854037642]
Moist Heat or Steam Sterilization
[20845854037642]
Moist Heat or Steam Sterilization
[20845854037642]
Moist Heat or Steam Sterilization
[20845854037642]
Moist Heat or Steam Sterilization
[20845854037642]
Moist Heat or Steam Sterilization
[20845854037642]
Moist Heat or Steam Sterilization
[20845854037642]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2022-09-16 |
Device Publish Date | 2020-09-24 |
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30845854027862 - GENESYS PressFT, Hi-Fi | 2024-04-25 GENESYS PressFT 2.1 w/One #2 (5 metric) Hi-Fi Suture, HIP (1 White/Black) |
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30845854034600 - GENESYS CrossFT, Hi-Fi | 2024-04-25 GENESYS CrossFT 5.5 mm Suture Anchor, w/3 Hi-Fi #2 (5 metric) Sutures w/Needles |
30845854034617 - GENESYS CrossFT, Hi-Fi | 2024-04-25 GENESYS CrossFT 6.5 mm Suture Anchor, w/2 Hi-Fi #2 (5 metric) Sutures w/Needles |
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