FDA UDI Not in Commercial Distribution 🇺🇸 United States

FMS

DI: 10886705023622 · Model: 283589 · DEPUY MITEK, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FMS
Primary DI
10886705023622
Version / Model
283589
Catalog Number
283589
Company Name
DEPUY MITEK, LLC
Labeler DUNS
190572854
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-01-30
Public Version
5
Public Version Date
2021-01-28
Public Version Status
Update
Public Device Record Key
97bba651-3ec2-4335-a593-f574ebd226c0
Distribution End Date
2021-01-28

Device Description

FMS INFLOW/OUTFLOW SHEATH Obturator Inflow/Outflow-Olympus

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
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
NBH ACCESSORIES,ARTHROSCOPIC

GMDN Terms

Code Name
33997 Surgical drill guide obturator

Identifiers

Type ID
Primary 10886705023622

Customer Contacts