FDA UDI In Commercial Distribution 🇺🇸 United States

RetroFit Sterile Disposable Needle Guide

DI: 00841912103355 · Model: 5300 · PROTEK MEDICAL PRODUCTS, INC.
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RetroFit Sterile Disposable Needle Guide
Primary DI
00841912103355
Version / Model
5300
Company Name
PROTEK MEDICAL PRODUCTS, INC.
Labeler DUNS
965417181
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
10
Public Version Date
2024-02-16
Public Version Status
Update
Public Device Record Key
40a356d2-a267-4251-9389-45cc4d3daf3c

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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KKX Drape, Surgical
ITX Transducer, Ultrasonic, Diagnostic

GMDN Terms

Code Name
44713 Body-surface ultrasound imaging transducer cover
45018 Needle guide, single-use

Identifiers

Type ID
Primary 00841912103355

Premarket Submissions

Submission Number Supplement Number
K970893 000
K973958 000