| Primary Device ID | 30845854035935 |
| NIH Device Record Key | 577f7cbb-df9a-407c-b6d9-5b34d10d3950 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | HD1001 |
| Catalog Number | HD1001 |
| Company DUNS | 071595540 |
| Company Name | Conmed 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 | false |
| Lot Batch | false |
| Serial Number | true |
| 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(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM |
| Outer Diameter | 10 Millimeter |
| Angle | 0 degree |
| Outer Diameter | 10 Millimeter |
| Angle | 0 degree |
| Outer Diameter | 10 Millimeter |
| Outer Diameter | 10 Millimeter |
| Outer Diameter | 10 Millimeter |
| Outer Diameter | 10 Millimeter |
| Outer Diameter | 10 Millimeter |
| 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 | 20845854035938 [Primary] |
| GS1 | 30845854035935 [Direct Marking] |
| GCJ | Laparoscope, general & plastic surgery |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[30845854035935]
Moist Heat or Steam Sterilization
[30845854035935]
Moist Heat or Steam Sterilization
[30845854035935]
Moist Heat or Steam Sterilization
[30845854035935]
Moist Heat or Steam Sterilization
[30845854035935]
Moist Heat or Steam Sterilization
[30845854035935]
Moist Heat or Steam Sterilization
[30845854035935]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-24 |
| 30653405033251 - ULTRACLEAN | 2026-03-25 ULTRACLEAN ACCESSORY ELECTRODE, 1 INCH COATED NEEDLE WITH EXTENDED INSULATION |
| 20845854035594 - CONCEPT | 2026-03-25 CONCEPT ABLATOR ELECTRODE, 90 DEGREE (ELECTRODE ONLY), QTY 5 |
| 30653405013925 - CONMED | 2026-03-24 ELECTROSURGICAL HANDPIECE SHEATH |
| 30653405014953 - POOLE | 2026-03-24 POOLE Suction Instrument with Removable Sheath and 10' (3.0 m) Clear Plastic Tubing |
| 30810175502367 - IBS-B | 2026-03-19 NON-BEVELED SCREWDRIVER T15- AO ATTACHMENT |
| 30653405546508 - Y-KnotlessTM Flex | 2026-02-16 Y-KnotlessTM Flex Anchor, Green/Black #2 Hi-Fi Suture, 1.8 mm |
| 30653405990721 - Y-KnotlessTM Flex | 2026-02-16 Y-KnotlessTM Flex Anchor, White/Black #2 Hi-Fi Suture, 1.8 mm |
| 10653405986362 - CONMED | 2026-01-26 Universal Modular Base Cart |