FDA UDI In Commercial Distribution 🇺🇸 United States

Prelude®

DI: 10884450010584 · Model: 10884450010584 · Merit Medical Systems, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
Prelude®
Primary DI
10884450010584
Version / Model
10884450010584
Company Name
Merit Medical Systems, Inc.
Labeler DUNS
184763290
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2016-09-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
08604f39-8ebb-4823-a19b-ac82a1b64420

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
38128 Vascular dilator, single-use

Identifiers

Type ID
Package 20884450010581
Primary 10884450010584
Unit of Use 00884450010587

Device Sizes

Type Value Unit Text
Device Size Text, specify Guide Wire Diameter-0.035" (0.89 mm)
Device Size Text, specify Sheath Length (cm)-23 cm (9")
Device Size Text, specify Sheath French Size (F)-7F