FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10845854026182 · Model: 9837 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10845854026182
Version / Model
9837
Catalog Number
9837
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-24
Public Version
2
Public Version Date
2022-09-26
Public Version Status
Update
Public Device Record Key
bc3b0302-1988-491f-a832-36901447c7f1

Device Description

HIP ARTHROSCOPY CANNULATED REUSABLE OBTURATOR 8.0 X 120MM

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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
35692 Rigid endoscope obturator

Identifiers

Type ID
Direct Marking 20845854026189
Primary 10845854026182

Customer Contacts

Device Sizes

Type Value Unit Text
Length 120 Millimeter
Outer Diameter 8 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY