| Primary Device ID | 08698870319562 |
| NIH Device Record Key | 391177c2-e6bb-4bac-80a0-cb7ce553dbac |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FMT |
| Version Model Number | E202-5060/GI |
| Company DUNS | 566222169 |
| Company Name | METKO MEDIKAL VE TIBBI CIHAZLAR DIS TICARET LIMITED SIRKETI |
| 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 | true |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 415 802-4021 |
| burcufirat@metkoltd.com | |
| Phone | 415 802-4021 |
| burcufirat@metkoltd.com | |
| Phone | 415 802-4021 |
| burcufirat@metkoltd.com | |
| Phone | 415 802-4021 |
| burcufirat@metkoltd.com | |
| Phone | 415 802-4021 |
| burcufirat@metkoltd.com | |
| Phone | 415 802-4021 |
| burcufirat@metkoltd.com | |
| Phone | 415 802-4021 |
| burcufirat@metkoltd.com | |
| Phone | 415 802-4021 |
| burcufirat@metkoltd.com | |
| Phone | 415 802-4021 |
| burcufirat@metkoltd.com | |
| Phone | 415 802-4021 |
| burcufirat@metkoltd.com | |
| Phone | 415 802-4021 |
| burcufirat@metkoltd.com | |
| Phone | 415 802-4021 |
| burcufirat@metkoltd.com | |
| Phone | 415 802-4021 |
| burcufirat@metkoltd.com | |
| Phone | 415 802-4021 |
| burcufirat@metkoltd.com | |
| Phone | 415 802-4021 |
| burcufirat@metkoltd.com | |
| Phone | 415 802-4021 |
| burcufirat@metkoltd.com |
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
| Storage Environment Temperature | Between 0 Degrees Celsius and 50 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08698870319562 [Primary] |
| IKD | Cable, Electrode |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2024-06-06 |
| Device Publish Date | 2020-05-22 |
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