FDA UDI In Commercial Distribution 🇺🇸 United States

Prelude®

DI: 10884450023751 · Model: 10884450023751 · Merit Medical Systems, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Prelude®
Primary DI
10884450023751
Version / Model
10884450023751
Catalog Number
OBT-4F-11
Company Name
Merit Medical Systems, Inc.
Labeler DUNS
184763290
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
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
03e89ac3-d867-4f16-8b9d-8d2e8fadf629

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 20884450023758
Primary 10884450023751
Unit of Use 00884450023754