FDA UDI In Commercial Distribution 🇺🇸 United States

NEUWAVE

DI: 00853719006364 · Model: LK15XT · NEUWAVE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NEUWAVE
Primary DI
00853719006364
Version / Model
LK15XT
Catalog Number
LK15XT
Company Name
NEUWAVE MEDICAL, INC.
Labeler DUNS
809758878
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-04-13
Public Version
6
Public Version Date
2023-10-18
Public Version Status
Update
Public Device Record Key
9a0003b3-25bf-42fc-b506-3d9d42892831

Device Description

NEUWAVE LK XT Probe 15CM 15ga

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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
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
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
NEY SYSTEM, ABLATION, MICROWAVE AND ACCESSORIES

GMDN Terms

Code Name
61286 Microwave ablation system probe, non-powered

Identifiers

Type ID
Primary 00853719006364
Package 10853719006361

Customer Contacts

Storage Conditions

Type
Handling Environment Humidity
Temperature Range
10 – 90 Percent (%) Relative Humidity
Type
Handling Environment Temperature
Temperature Range
-22 – 60 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
Do not use if package is damaged