FDA UDI In Commercial Distribution 🇺🇸 United States

CATALYSTEM

DI: 00885556892114 · Model: 71314201 · Smith & Nephew, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
CATALYSTEM
Primary DI
00885556892114
Version / Model
71314201
Catalog Number
71314201
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-07-30
Public Version
1
Public Version Date
2024-08-07
Public Version Status
New
Public Device Record Key
3e3fa04f-88f9-4ca8-986b-18346ba5787c

Device Description

CATALYSTEM BROACH SIZE 1

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
Moist Heat or Steam Sterilization

Product Codes

Code Name
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
MEH Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented

GMDN Terms

Code Name
36167 Orthopaedic broach

Identifiers

Type ID
Primary 00885556892114

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K123598 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Size 1