FDA UDI In Commercial Distribution 🇺🇸 United States

FIBER LARYNGOSCOPE

DI: 04961333232789 · Model: FNL-15RP3 · PENTAX OF AMERICA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FIBER LARYNGOSCOPE
Primary DI
04961333232789
Version / Model
FNL-15RP3
Company Name
PENTAX OF AMERICA, INC.
Labeler DUNS
083211284
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-04-06
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
d528e892-9d1b-4170-96e1-055033b39c15

Device Description

FIBER NASO PHARYNGO LARYNGOSCOPE (REFURBISHED)

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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Ethylene Oxide", "High-level Disinfectant"]

Product Codes

Code Name
EOB Nasopharyngoscope (Flexible Or Rigid)

GMDN Terms

Code Name
44715 Flexible fibreoptic nasopharyngolaryngoscope

Identifiers

Type ID
Primary 04961333232789

Premarket Submissions

Submission Number Supplement Number
K921707 000