FDA UDI In Commercial Distribution 🇺🇸 United States

GlideScope®

DI: 00879123008596 · Model: GlideScope® Core™ 15 FHD · Verathon Medical (Canada) ULC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
GlideScope®
Primary DI
00879123008596
Version / Model
GlideScope® Core™ 15 FHD
Catalog Number
0570-0437
Company Name
Verathon Medical (Canada) ULC
Labeler DUNS
243738320
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-04-20
Public Version
1
Public Version Date
2023-04-28
Public Version Status
New
Public Device Record Key
488905d8-b35e-4536-8ce4-e8ac7006c6c4

Device Description

GlideScope® Core™ 15 FHD Monitor

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
CCW Laryngoscope, Rigid

GMDN Terms

Code Name
36612 Image display unit, colour

Identifiers

Type ID
Package 10879123008593
Primary 00879123008596