FDA UDI Not in Commercial Distribution 🇺🇸 United States

FMS

DI: 10886705016440 · Model: 282000 · DEPUY MITEK, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FMS
Primary DI
10886705016440
Version / Model
282000
Catalog Number
282000
Company Name
DEPUY MITEK, LLC
Labeler DUNS
190572854
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-01
Public Version
5
Public Version Date
2021-09-17
Public Version Status
Update
Public Device Record Key
2c4c9e3b-cf0b-40a0-901c-77e7cd4190ca
Distribution End Date
2021-01-28

Device Description

FMS Hand Control Interface To Arthrex Adapteur Power System II

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
No

Product Codes

Code Name
HRX ARTHROSCOPE

GMDN Terms

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

Identifiers

Type ID
Primary 10886705016440

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K954465 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Waste from Electrical and Electronic Equipment