FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 04961333240517 · Model: 8861 · PENTAX OF AMERICA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
04961333240517
Version / Model
8861
Company Name
PENTAX OF AMERICA, INC.
Labeler DUNS
083211284
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-02-26
Public Version
4
Public Version Date
2023-11-17
Public Version Status
Update
Public Device Record Key
5fef6366-ba1f-4416-b964-3f7adeeb3a5e

Device Description

ADAPTABLE TUBE, 70 DEG

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Moist Heat or Steam Sterilization", "High-level Disinfectant"]

Product Codes

Code Name
EOB Nasopharyngoscope (Flexible Or Rigid)

GMDN Terms

Code Name
35205 Rigid optical nasopharyngoscope

Identifiers

Type ID
Primary 04961333240517

Premarket Submissions

Submission Number Supplement Number
K944656 000

Device Sizes

Type Value Unit Text
Angle 70.0 degree