FDA UDI In Commercial Distribution 🇺🇸 United States

FIBER INTUBATION SCOPE

DI: 04961333240289 · Model: FI-10RBS · PENTAX OF AMERICA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FIBER INTUBATION SCOPE
Primary DI
04961333240289
Version / Model
FI-10RBS
Company Name
PENTAX OF AMERICA, INC.
Labeler DUNS
083211284
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-03-12
Public Version
1
Public Version Date
2018-04-12
Public Version Status
New
Public Device Record Key
c55d7641-d0f2-458b-8d4b-64e4d9f65c86

Device Description

FIBEROPTICINTUBATIONSCOPE 1.4C 3.4TP ROP (USED)

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
Yes
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
["Ethylene Oxide", "High-level Disinfectant"]

Product Codes

Code Name
CAL Laryngoscope, Non-Rigid

GMDN Terms

Code Name
36706 Flexible fibreoptic intubation laryngoscope

Identifiers

Type ID
Primary 04961333240289