FDA UDI In Commercial Distribution 🇺🇸 United States

Non-Sterile Latex Endocavity Probe Cover

DI: 10841912100900 · Model: 3232 · PROTEK MEDICAL PRODUCTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
24

Basic Information

Brand Name
Non-Sterile Latex Endocavity Probe Cover
Primary DI
10841912100900
Version / Model
3232
Catalog Number
3232
Company Name
PROTEK MEDICAL PRODUCTS, INC.
Labeler DUNS
965417181
Distribution Status
In Commercial Distribution
Device Count in Pkg
24
Record Status
Published
Publish Date
2016-09-16
Public Version
4
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
920d41eb-54f1-4d2a-90e0-c438f6e7560d

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KKX Drape, Surgical

GMDN Terms

Code Name
60609 Body-orifice ultrasound imaging transducer cover, basic, non-sterile

Identifiers

Type ID
Primary 10841912100900
Unit of Use 00841912100903

Premarket Submissions

Submission Number Supplement Number
K970891 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight