FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10705034507422 · Model: 163010515 · Medos International Sàrl
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10705034507422
Version / Model
163010515
Catalog Number
163010515
Company Name
Medos International Sàrl
Labeler DUNS
482661753
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-13
Public Version
5
Public Version Date
2021-12-30
Public Version Status
Update
Public Device Record Key
1bd37840-c095-4bc6-9ea8-3edc9af95c6d

Device Description

CONCORDE Clear MIS DISCECTOMY DEVICE LONG 5MM, 15 DEGREES

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
No
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
HRX ARTHROSCOPE

GMDN Terms

Code Name
35917 Surgical/emergency suction cannula, non-illuminating, single-use

Identifiers

Type ID
Primary 10705034507422

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K122861 000