FDA UDI Not in Commercial Distribution 🇺🇸 United States

FASTPAK

DI: 00885556747643 · Model: 74013710 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
FASTPAK
Primary DI
00885556747643
Version / Model
74013710
Catalog Number
74013710
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-06-13
Public Version
2
Public Version Date
2024-10-16
Public Version Status
Update
Public Device Record Key
7e9c649b-1adf-4972-949a-2815effde7b3
Distribution End Date
2024-10-15

Device Description

JOURNEY II FASTPAK FEMORAL TRIAL, CAM MODULE, NOTCH TRIAL LEFT SIZE 10

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

GMDN Terms

Code Name
66185 Knee femur prosthesis trial, single-use

Identifiers

Type ID
Primary 00885556747643

Customer Contacts