MICROLAP
- Primary DI
- 20653405037504
- Brand
- MICROLAP
- Company
- Conmed Corporation
- Model
- MK-1500
- Catalog number
- MK-1500
- Device description
- Primary Second Site Introducer with Insufflation Needle
- 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
- OTC
- false
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| HET | LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES) |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| HET | Laparoscope, Gynecologic (And Accessories) | Obstetrics/Gynecology | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K943810 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 20653405037504 | Package | GS1 | 10 | Not in Commercial Distribution |
| 30653405037501 | Primary | GS1 | 0 | |
| 00653405037500 | Unit of Use | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 20653405037504 | 20653405037504 | ||
| 30653405037501 | 30653405037501 | ||
| 00653405037500 | 00653405037500 | 653405037500 | 0653405037500 |
GMDN Terms#
| Term | Definition |
|---|---|
| Spring-loaded pneumoperitoneum needle, single-use | A slender, sharply-pointed metal tube designed to introduce or remove gas from the peritoneal cavity as a therapeutic or surgical/radiological procedural method. It is often inserted into the peritoneal cavity for the purpose of insufflation [e.g., with carbon dioxide (CO2)] to establish pneumoperitoneum prior to abdominal endoscopy. It is equipped with a spring-loaded, round-tipped obturator that extends from the tube when the device does not encounter resistance (i.e., when the cavity has been reached) to prevent damage from the sharp point. This is a single-use device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 | |
| 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 |
|---|
| Ethylene Oxide |
Contacts#
| Phone | |
|---|---|
| +1(800)237-0169 | CUSTOMER_SERVICE@CONMED.COM |
Regulatory Flags#
- DUNS number
- 071595540
- Device count
- 10
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
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