FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 20845854018863 · Model: HA-222DK · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
20845854018863
Version / Model
HA-222DK
Catalog Number
HA-222DK
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-10-14
Public Version
1
Public Version Date
2021-10-22
Public Version Status
New
Public Device Record Key
f7c1ad17-016f-4538-9d94-8b2b7469f093

Device Description

HIP Arthroscopy Disposable Kit

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
Yes
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
KDD Kit, surgical instrument, disposable

GMDN Terms

Code Name
44093 Arthroscopic surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Primary 20845854018863

Customer Contacts