GEMINI
- Primary DI
- 03596010113702
- Brand
- GEMINI
- Company
- Smith & Nephew, Inc.
- Model
- 3004
- Catalog number
- 3004
- Device description
- 2.0 MM X 8 FEET UNIVERSAL FIBER OPTIC LIGHT CABLES WITH SMITH and NEPHEW/WOLF ADAPTORS. FOR USE WITH 1.9 MM ARTHROSCOPES
- Published
- 2015-08-30
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| GCJ | Laparoscope, general & plastic surgery |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| GCJ | Laparoscope, General & Plastic Surgery | Gastroenterology, Urology | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K914919 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 03596010113702 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 03596010113702 | 03596010113702 | 3596010113702 |
GMDN Terms#
| Term | Definition |
|---|---|
| Electrical-only medical device connection cable, reusable | A non-patient-contact, insulated, electrical cord with a connector (plug) at both ends designed to transmit electrical power and/or signal (data) between medical devices (e.g., to connect a lead, electrical catheter, handpiece, or monitor to a parent device). It is not intended to connect directly to patient-worn electrodes (i.e., it is not a lead), is not intended to connect to the mains (i.e., not a mains power cable), does not generate any type of power and/or signal, and has no additional non-electrical conducting or processing functionality. This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(800)821-5700 | gudid@smith-nephew.com |
| +1(800)238-7538 | GUDID@SMITH-NEPHEW.COM |
Regulatory Flags#
- DUNS number
- 045483575
- Device count
- 1
- Lot or batch
- true
- Serial number
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 03596010619952 | NA | 72201597 | 72201597 | 2015-08-29 |
| 03596010619969 | NA | 72201598 | 72201598 | 2015-08-29 |
| 00885556572351 | NA | 72201597S | 72201597S | 2017-06-15 |
| 00885556572368 | NA | 72201598S | 72201598S | 2017-06-15 |
| 00885556830543 | PyroCarbon Modular Radial Head | TRL-310-01 | TRL-310-01 | 2026-09-24 |
| 00885556830550 | PyroCarbon Modular Radial Head | TRL-310-02 | TRL-310-02 | 2026-09-24 |
| 00885556830567 | PyroCarbon Modular Radial Head | TRL-310-03 | TRL-310-03 | 2026-09-24 |
| 00885556830574 | PyroCarbon Modular Radial Head | TRL-310-04 | TRL-310-04 | 2026-09-24 |
| 00885556839690 | Total Foot System 2 | CSA-800-06 | CSA-800-06 | 2026-09-24 |
| 00885556839706 | Total Foot System 2 | CSA-800-07 | CSA-800-07 | 2026-09-24 |
| 00885556854778 | Cadence Total Ankle System | CSA-1020-0014 | CSA-1020-0014 | 2026-09-24 |
| 00885556859636 | Titan Modular Shoulder System | CSA092009 | CSA092009 | 2026-09-24 |
| 00885556859643 | Titan Modular Shoulder System | CSA092010 | CSA092010 | 2026-09-24 |
| 00885556859650 | Titan Modular Shoulder System | CSA092011 | CSA092011 | 2026-09-24 |
| 00885556859698 | Titan Modular Shoulder System | CSA-0920-15 | CSA-0920-15 | 2026-09-24 |
| 00885556859704 | Titan Modular Shoulder System | CSA-0920-16 | CSA-0920-16 | 2026-09-24 |
| 00885556859711 | Titan Modular Shoulder System | CSA-0920-17 | CSA-0920-17 | 2026-09-24 |
| 00885556859728 | Titan Modular Shoulder System | CSA-0920-18 | CSA-0920-18 | 2026-09-24 |
| 00885556859735 | Titan Modular Shoulder System | CSA-0920-19 | CSA-0920-19 | 2026-09-24 |
| 00885556859742 | Titan Modular Shoulder System | CSA-0920-20 | CSA-0920-20 | 2026-09-24 |
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