FDA UDI In Commercial Distribution 🇺🇸 United States

CrossFix®

DI: M543CM8001 · Model: CM-8001 · CAYENNE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
CrossFix®
Primary DI
M543CM8001
Version / Model
CM-8001
Company Name
CAYENNE MEDICAL, INC.
Labeler DUNS
606719685
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-23
Public Version
7
Public Version Date
2025-05-30
Public Version Status
Update
Public Device Record Key
538d3687-8965-4640-ad6a-6c7f6e2c4b82

Device Description

CrossFix® All-Suture Meniscal Repair, straight

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 M543CM8001