FDA UDI In Commercial Distribution 🇺🇸 United States

GlideScope®

DI: 00879123005304 · Model: Spectrum™ LoPro S2 · Verathon Medical (Canada) ULC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
GlideScope®
Primary DI
00879123005304
Version / Model
Spectrum™ LoPro S2
Catalog Number
0574-0166
Company Name
Verathon Medical (Canada) ULC
Labeler DUNS
243738320
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-08
Public Version
2
Public Version Date
2022-12-20
Public Version Status
Update
Public Device Record Key
21c62920-8a03-40af-85bb-e992f8aa7999

Device Description

GlideScope® Spectrum™ LoPro S2

Device Characteristics

Single Use
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
CCW Laryngoscope, Rigid

GMDN Terms

Code Name
62760 Video intubation laryngoscope blade

Identifiers

Type ID
Primary 00879123005304
Package 10879123005301