FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 20845854605933 · Model: UQL6130 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
20845854605933
Version / Model
UQL6130
Catalog Number
UQL6130
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-03-25
Public Version
3
Public Version Date
2023-10-13
Public Version Status
Update
Public Device Record Key
3429fd0f-7bab-46a9-b824-1cd06d5aa80f
Distribution End Date
2023-10-12

Device Description

5.9 MM, QUICKLATCH SHEATH BODY 157 MM WL

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
NBH ACCESSORIES,ARTHROSCOPIC

GMDN Terms

Code Name
44091 Arthroscopic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Direct Marking 30845854605930
Primary 20845854605933

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 5.9 MM

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-4 – 140 Degrees Fahrenheit
Type
Storage Environment Humidity
Temperature Range
10 – 90 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-20 – 60 Degrees Celsius