FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886705003532 · Model: 214112 · DEPUY MITEK, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886705003532
Version / Model
214112
Catalog Number
214112
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
3
Public Version Date
2020-07-22
Public Version Status
Update
Public Device Record Key
ced3f6a9-655c-4e68-a1c7-4e333003b58d

Device Description

THREADED CLEAR CANNULA WITH OBTURATOR 7mm x 110mm

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
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEA CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY

GMDN Terms

Code Name
58752 Arthroscopic access cannula, single-use

Identifiers

Type ID
Package 20886705003539
Primary 10886705003532

Customer Contacts