FDA UDI In Commercial Distribution 🇺🇸 United States

NovoStitch

DI: 00853541006105 · Model: CTX-R001 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NovoStitch
Primary DI
00853541006105
Version / Model
CTX-R001
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-07
Public Version
7
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
a43c645a-43cc-4068-a8e9-66bfe246f8b5

Device Description

NovoStitch Meniscal Repair Cartridge

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GAT Suture, Nonabsorbable, Synthetic, Polyethylene

GMDN Terms

Code Name
13907 Polyolefin/fluoropolymer suture, multifilament

Identifiers

Type ID
Primary 00853541006105

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K063778 000