FDA UDI Not in Commercial Distribution 🇺🇸 United States

UltraPoint™

DI: 10816843022591 · Model: 016395 · ROCHESTER ELECTRO-MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
UltraPoint™
Primary DI
10816843022591
Version / Model
016395
Company Name
ROCHESTER ELECTRO-MEDICAL, INC.
Labeler DUNS
068156330
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
4
Public Version Date
2019-05-21
Public Version Status
Update
Public Device Record Key
11ef7c23-6047-45e5-8725-fe876bd63f38
Distribution End Date
2019-05-20

Device Description

DISPOSABLE ULTRAPOINT MONOPOLAR NEEDLE ELECTRODES: 26 GA., 50 MM NEEDLE, 2 FT. (0.6 M) SINGLE GREEN LEADWIRE

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
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
IKT Electrode, Needle, Diagnostic Electromyograph

GMDN Terms

Code Name
11441 Electromyographic needle electrode, single-use

Identifiers

Type ID
Primary 10816843022591
Package 10816843022584

Customer Contacts

Phone
18003285544