FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 20845854061449 · Model: 0620-030-100 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
NA
Primary DI
20845854061449
Version / Model
0620-030-100
Catalog Number
0620-030-100
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2020-09-29
Public Version
1
Public Version Date
2020-10-07
Public Version Status
New
Public Device Record Key
03cd9cda-ab43-420e-9d71-e61dadd7d8fb

Device Description

Active Laparoscopic Plume Filtration Device

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
Yes
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
Radiation Sterilization

Product Codes

Code Name
NKC Tubing/tubing with filter, insufflation, laparoscopic

GMDN Terms

Code Name
46483 Surgical plume evacuation system tube

Identifiers

Type ID
Package 30845854061446
Primary 20845854061449
Unit of Use 00845854061445

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
14 – 104 Degrees Fahrenheit
Type
Storage Environment Temperature
Temperature Range
-10 – 40 Degrees Celsius