FDA UDI In Commercial Distribution 🇺🇸 United States

Prelude® PRO

DI: 10884450708337 · Model: F · Merit Medical Systems, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
Prelude® PRO
Primary DI
10884450708337
Version / Model
F
Catalog Number
PRO-5F-11-038
Company Name
Merit Medical Systems, Inc.
Labeler DUNS
184763290
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2024-02-16
Public Version
1
Public Version Date
2024-02-26
Public Version Status
New
Public Device Record Key
4c24eeff-537b-4580-8d17-ed5d9b782ea0

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
DRE DILATOR, VESSEL, FOR PERCUTANEOUS CATHETERIZATION

GMDN Terms

Code Name
58865 Vascular catheter introduction set, nonimplantable

Identifiers

Type ID
Package 20884450708334
Primary 10884450708337
Unit of Use 00884450708330

Device Sizes

Type Value Unit Text
Device Size Text, specify Guide Wire Diameter-0.038" (0.97 mm)
Device Size Text, specify Sheath French Size (F)-5F
Device Size Text, specify Sheath Length (cm)-11 cm (4.3")