FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10845854034019 · Model: C7385 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10845854034019
Version / Model
C7385
Catalog Number
C7385
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
1
Public Version Date
2020-10-02
Public Version Status
New
Public Device Record Key
f43196a9-084e-4f66-af61-45d511ac583f

Device Description

7.0 X 85MM REUSABLE OBTURATOR

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
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
35692 Rigid endoscope obturator

Identifiers

Type ID
Direct Marking 20845854034016
Primary 10845854034019

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 7 Millimeter
Length 85 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY