REFLEX
- Primary DI
- 10653405035138
- Brand
- REFLEX
- Company
- Conmed Corporation
- Model
- 1802
- Catalog number
- 1802
- Device description
- REFLEX 10/12MM SITE STABILITY DEVICE
- Published
- 2016-09-24
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Sterile
- true
- Single use
- 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 |
|---|---|
| K924761 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10653405035138 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 10653405035138 | 10653405035138 |
GMDN Terms#
| Term | Definition |
|---|---|
| Laparoscopic access cannula seal reducer | A small device intended to reduce the sealing diameter of an existing laparoscopic access cannula seal, so laparoscopic instruments with smaller diameters can be introduced through the parent laparoscopic sleeve whilst maintaining a seal and inhibiting the leakage of insufflation media [e.g., carbon dioxide (CO2) gas]. It is intended to fit within the laparoscopic access cannula seal (fitted at the proximal end of the cannula) when required throughout the laparoscopic surgical procedure. This is a single-use device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Storage Environment Temperature | 10 Degrees Celsius | 32 Degrees Celsius | |
| Storage Environment Temperature | 50 Degrees Fahrenheit | 90 Degrees Fahrenheit |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)237-0169 | CUSTOMER_SERVICE@CONMED.COM |
Regulatory Flags#
- DUNS number
- 071595540
- Device count
- 1
- Lot or batch
- true
- Expiration date on label
- true
- No natural rubber latex
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 20845854655501 | Argo Knotless | KBC475-KIT | KBC475-KIT | 2026-09-25 |
| 20845854655518 | Argo Knotless | K475-KIT | K475-KIT | 2026-09-25 |
| 30845854655478 | ConMed Airseal | SHELF-ICART | SHELF-ICART | 2026-09-18 |
| 20845854082482 | Paradigm | PEZS01A | PEZS01A | 2020-11-16 |
| 20845854015466 | SEQUENT | MR007C | MR007C | 2015-10-24 |
| 20845854036584 | SEQUENT | MR004C | MR004C | 2015-10-24 |
| 10653405044703 | CORE DYNAMICS | CD1406 | CD1406 | 2026-03-23 |
| 10653405045083 | CORE DYNAMICS | CD1608FH | CD1608FH | 2026-03-24 |
| 20653405990908 | GENESYS™ CrossFT™ | CFBC-4502R | CFBC-4502R | 2026-07-31 |
| 20653405990915 | GENESYS™ CrossFT™ | CFBC-4503R | CFBC-4503R | 2026-07-31 |
| 20653405990922 | GENESYS™ CrossFT™ | CFBC-5502R | CFBC-5502R | 2026-07-31 |
| 20653405990939 | GENESYS™ CrossFT™ | CFBC-5503R | CFBC-5503R | 2026-07-31 |
| 20653405990946 | GENESYS™ CrossFT™ | CFBC-6502R | CFBC-6502R | 2026-07-31 |
| 20653405990953 | GENESYS™ CrossFT™ | CFBC-6503R | CFBC-6503R | 2026-07-31 |
| 10653405000242 | YANKAUER | 0034470 | 0034470 | 2016-09-24 |
| 10845854035559 | E9000 | E9015 | E9015 | 2026-03-24 |
| 20653405008559 | CONMED | 60-0824-001 | 60-0824-001 | 2016-09-24 |
| 30653405003230 | CONMED | 138011 | 138011 | 2016-09-24 |
| 30653405003247 | CONMED | 138012 | 138012 | 2016-09-24 |
| 30653405058230 | AER DEFENSE | 60-8084-001 | 60-8084-001 | 2016-09-24 |
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