FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10653405005766 · Model: 9707 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
NA
Primary DI
10653405005766
Version / Model
9707
Catalog Number
9707
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2022-06-03
Public Version
1
Public Version Date
2022-06-13
Public Version Status
New
Public Device Record Key
cbb787a3-2d8f-4e6e-b835-9f3aa940cc0c

Device Description

CAMERA DRAPE 9 IN. X 95 IN.

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
No

Product Codes

Code Name
KKX Drape, surgical

GMDN Terms

Code Name
47487 Electrical-only medical device connection cable, reusable

Identifiers

Type ID
Package 20653405005763
Primary 10653405005766
Unit of Use 00653405005769

Customer Contacts