FDA UDI In Commercial Distribution 🇺🇸 United States

GlideScope®

DI: 00879123006233 · Model: Spectrum™ LoPro S4 · Verathon Medical (Canada) ULC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
GlideScope®
Primary DI
00879123006233
Version / Model
Spectrum™ LoPro S4
Catalog Number
0574-0195
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
5ac09901-c575-44ad-bc93-5b9b3a9fc5da

Device Description

GlideScope® Spectrum™ LoPro S4

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
Package 10879123006230
Primary 00879123006233