FDA UDI In Commercial Distribution 🇺🇸 United States

TorFlex Transseptal Guiding Sheath

DI: 00685447005476 · Model: TF85-32-81-135 · Baylis Médicale Cie Inc
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TorFlex Transseptal Guiding Sheath
Primary DI
00685447005476
Version / Model
TF85-32-81-135
Company Name
Baylis Médicale Cie Inc
Labeler DUNS
249225954
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-11-01
Public Version
5
Public Version Date
2023-12-08
Public Version Status
Update
Public Device Record Key
2bcc5d11-3e42-473d-945e-941eff6dfe26

Device Description

TorFlex Transseptal Sheath; Transseptal Dilator; J-Tip Guidewire

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DYB Introducer, Catheter
DQY Catheter, Percutaneous
DRE Dilator, Vessel, For Percutaneous Catheterization

GMDN Terms

Code Name
17846 Vascular guide-catheter, single-use

Identifiers

Type ID
Primary 00685447005476

Device Sizes

Type Value Unit Text
Device Size Text, specify 81cm 8.5F TorFlex Transseptal Sheath with 135° curve; 85cm 8.5F Transseptal Dilator; 180cm J-Tip Guidewire with OD = 0.032 inch; Max Guidewire OD = 0.032 inch