FDA UDI Not in Commercial Distribution 🇺🇸 United States

MICROPOWER

DI: 20845854013189 · Model: 6021-021 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MICROPOWER
Primary DI
20845854013189
Version / Model
6021-021
Catalog Number
6021-021
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
5
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
0649f376-e160-4cc8-bc3c-8c7dbdfb1899
Distribution End Date
2022-06-09

Device Description

MICROPOWER MEDIUM SPEED DRILL, PERMANENT LEVER

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
No
Has Serial Number
Yes
Has Lot/Batch Number
No
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
HRX ARTHROSCOPE

GMDN Terms

Code Name
44491 Multi-purpose surgical power tool system, line-powered

Identifiers

Type ID
Direct Marking 30845854013186
Primary 20845854013189

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K072706 000