FDA UDI In Commercial Distribution 🇺🇸 United States

EXPRESS

DI: 03700879512204 · Model: 139-00-0002 · NOVASTEP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EXPRESS
Primary DI
03700879512204
Version / Model
139-00-0002
Catalog Number
139-00-0002
Company Name
NOVASTEP
Labeler DUNS
264255288
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-18
Public Version
5
Public Version Date
2024-02-08
Public Version Status
Update
Public Device Record Key
09655e50-21f1-4927-a000-a761993cc4f5

Device Description

Staple Tray - Hindfoot

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
Yes
Has Serial Number
Yes
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
FSM Tray, Surgical, Instrument

GMDN Terms

Code Name
13730 Device sterilization/disinfection container, reusable

Identifiers

Type ID
Primary 03700879512204

Customer Contacts

Phone
+33299338650