FDA UDI In Commercial Distribution 🇺🇸 United States

eXpress®

DI: 03700879502083 · Model: 139-00-0030 · NOVASTEP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
eXpress®
Primary DI
03700879502083
Version / Model
139-00-0030
Catalog Number
139-00-0030
Company Name
NOVASTEP
Labeler DUNS
264255288
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-04-15
Public Version
3
Public Version Date
2024-02-08
Public Version Status
Update
Public Device Record Key
f2382f80-7b12-4dc7-a166-e8d6f54bdbb0

Device Description

Ø3mm Solid Drill

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
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
HWE Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 03700879502083

Customer Contacts

Phone
+33299338650