FDA UDI In Commercial Distribution 🇺🇸 United States

FMS

DI: 10886705016358 · Model: 281583 · DEPUY MITEK, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
FMS
Primary DI
10886705016358
Version / Model
281583
Catalog Number
281583
Company Name
DEPUY MITEK, LLC
Labeler DUNS
190572854
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-01
Public Version
6
Public Version Date
2026-03-26
Public Version Status
Update
Public Device Record Key
b229084b-c51a-4672-8cc8-6029e572cdfc

Device Description

FMS Obturator for Cannulas 281580

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
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
High-level Disinfectant

Product Codes

Code Name
HRX ARTHROSCOPE

GMDN Terms

Code Name
46102 Surgical irrigation tubing set, single-use

Identifiers

Type ID
Primary 10886705016358

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K951843 000