FDA UDI Not in Commercial Distribution 🇺🇸 United States

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DI: 30653405033770 · Model: 60-6050-851 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
6

Basic Information

Brand Name
SELECT ONE
Primary DI
30653405033770
Version / Model
60-6050-851
Catalog Number
60-6050-851
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
6
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
4f6382e8-7cc8-4a18-b3cb-b2a37b6e1bd8
Distribution End Date
2020-12-08

Device Description

SELECT ONE LAPAROSCOPIC PROCEDURE PACK

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
["Radiation Sterilization", "Ethylene Oxide"]

Product Codes

Code Name
KOD CATHETER, UROLOGICAL

GMDN Terms

Code Name
44096 Laparoscopic surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Package 20653405033773
Primary 30653405033770
Unit of Use 00653405033779

Customer Contacts

Storage Conditions

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