FDA UDI In Commercial Distribution 🇺🇸 United States

Director Biopsy/Needle Guide/Probe Cover Kit

DI: 00841912101115 · Model: 4218 · PROTEK MEDICAL PRODUCTS, INC.
Product Codes
2
GMDN Terms
2
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Director Biopsy/Needle Guide/Probe Cover Kit
Primary DI
00841912101115
Version / Model
4218
Catalog Number
4218
Company Name
PROTEK MEDICAL PRODUCTS, INC.
Labeler DUNS
965417181
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-04-25
Public Version
10
Public Version Date
2024-02-16
Public Version Status
Update
Public Device Record Key
d5177ea8-528b-408b-8512-da6e93a8c2b9

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
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

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

GMDN Terms

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

Identifiers

Type ID
Package 10841912101112
Primary 00841912101115
Package 20841912101119

Premarket Submissions

Submission Number Supplement Number
K970893 000
K973958 000