FDA UDI In Commercial Distribution 🇺🇸 United States

GlideScope®

DI: 00879123008602 · Model: GlideScope® Core™ 15 FHD Premium Configuration · Verathon Medical (Canada) ULC
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GlideScope®
Primary DI
00879123008602
Version / Model
GlideScope® Core™ 15 FHD Premium Configuration
Catalog Number
0270-1030-FHD
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
53a35933-fc2e-4923-b1c3-975a79f6ac5f

Device Description

GlideScope® Core™ 15 FHD Premium Configuration with GlideScope QuickConnect™ Cable

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
47487 Electrical-only medical device connection cable, reusable

Identifiers

Type ID
Primary 00879123008602