FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 04961333241736 · Model: 100135P · PENTAX OF AMERICA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
N/A
Primary DI
04961333241736
Version / Model
100135P
Company Name
PENTAX OF AMERICA, INC.
Labeler DUNS
083211284
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2018-03-13
Public Version
2
Public Version Date
2018-07-06
Public Version Status
New
Public Device Record Key
83b49c46-78d0-468f-a5ad-ad436a49ed90

Device Description

BIOPSY TUBING,SINGLE USE PKG 10

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OCX Endoscopic Irrigation/Suction System

GMDN Terms

Code Name
47800 Surgical fluid/gas irrigator

Identifiers

Type ID
Primary 04961333241736
Unit of Use 14961333241733

Premarket Submissions

Submission Number Supplement Number
K060962 000