FDA UDI In Commercial Distribution 🇺🇸 United States

BFlex™

DI: 00879123008541 · Model: BFlex™ 2 Ultraslim 2.8 · Verathon Medical (Canada) ULC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
BFlex™
Primary DI
00879123008541
Version / Model
BFlex™ 2 Ultraslim 2.8
Catalog Number
0570-0434
Company Name
Verathon Medical (Canada) ULC
Labeler DUNS
243738320
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-04-03
Public Version
1
Public Version Date
2023-04-11
Public Version Status
New
Public Device Record Key
ae235517-68bb-4685-984d-34d4624ab717

Device Description

BFlex™ 2 Ultraslim 2.8 Single-Use Bronchoscope

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
No
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
EOQ Bronchoscope (Flexible Or Rigid)

GMDN Terms

Code Name
60963 Flexible video bronchoscope, single-use

Identifiers

Type ID
Package 10879123008548
Primary 00879123008541

Premarket Submissions

Submission Number Supplement Number
K211947 000