FDA UDI In Commercial Distribution 🇺🇸 United States

NikoSurg

DI: 10853512006599 · Model: 2508 · NIKOMED USA
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NikoSurg
Primary DI
10853512006599
Version / Model
2508
Catalog Number
2508
Company Name
NIKOMED USA
Labeler DUNS
073648341
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-01-17
Public Version
4
Public Version Date
2020-06-05
Public Version Status
Update
Public Device Record Key
34d6888d-2003-4e02-974b-928326420a05

Device Description

Neutral Electrodes

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
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
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, cutting & coagulation & accessories

GMDN Terms

Code Name
58494 Electrosurgical return electrode, single-use

Identifiers

Type ID
Primary 10853512006599
Package 30853512006593
Package 20853512006596

Customer Contacts

Phone
+1(800)355-6456 ext. 205

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
41 – 86 Degrees Fahrenheit