FDA UDI Not in Commercial Distribution 🇺🇸 United States

AIRLOCK

DI: 03700879509792 · Model: SUI05001 · NOVASTEP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AIRLOCK
Primary DI
03700879509792
Version / Model
SUI05001
Catalog Number
SUI05001
Company Name
NOVASTEP
Labeler DUNS
264255288
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-05
Public Version
3
Public Version Date
2023-09-04
Public Version Status
Update
Public Device Record Key
a1313324-4e17-4b32-a5aa-c7166bb783bc
Distribution End Date
2022-07-26

Device Description

Single Use Instrumentation Kit - Benders

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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 03700879509792

Customer Contacts

Phone
+33299338650