FDA UDI In Commercial Distribution 🇺🇸 United States

Reusable Stainless Steel Endocavity Needle Guide

DI: 10841912104861 · Model: 6256 · PROTEK MEDICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Reusable Stainless Steel Endocavity Needle Guide
Primary DI
10841912104861
Version / Model
6256
Company Name
PROTEK MEDICAL PRODUCTS, INC.
Labeler DUNS
965417181
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-13
Public Version
7
Public Version Date
2022-06-17
Public Version Status
Update
Public Device Record Key
dc400cad-a1f5-4ad3-9915-7249222d5559

Device Description

Stainless Steel Reusable Endocavity Needle Guide for Supersonic Imagine SE12-3

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
ITX Transducer, Ultrasonic, Diagnostic

GMDN Terms

Code Name
60734 Needle guide, reusable

Identifiers

Type ID
Direct Marking 00841912104864
Primary 10841912104861

Premarket Submissions

Submission Number Supplement Number
K971115 000
K971722 000