FDA UDI Not in Commercial Distribution 🇺🇸 United States

MICROLAP

DI: 30653405037518 · Model: MK-3500 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
MICROLAP
Primary DI
30653405037518
Version / Model
MK-3500
Catalog Number
MK-3500
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-09-24
Public Version
3
Public Version Date
2020-12-08
Public Version Status
Update
Public Device Record Key
9375346c-66ae-4c6e-8ac7-5ea4d087cfd0
Distribution End Date
2020-12-08

Device Description

3mm Introducer with Sterile Single-Use Insufflation Needle

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
HET LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES)

GMDN Terms

Code Name
12750 Spring-loaded pneumoperitoneum needle, single-use

Identifiers

Type ID
Package 20653405037511
Primary 30653405037518
Unit of Use 00653405037517

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Introducer

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
50 – 90 Degrees Fahrenheit
Type
Storage Environment Temperature
Temperature Range
10 – 32 Degrees Celsius