FDA UDI In Commercial Distribution 🇺🇸 United States

Xtractor

DI: 37290019371008 · Model: 1 · XCARDIA INNOVATION LTD
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
3

Basic Information

Brand Name
Xtractor
Primary DI
37290019371008
Version / Model
1
Company Name
XCARDIA INNOVATION LTD
Labeler DUNS
521798660
Distribution Status
In Commercial Distribution
Device Count in Pkg
3
Record Status
Published
Publish Date
2022-04-25
Public Version
1
Public Version Date
2022-05-03
Public Version Status
New
Public Device Record Key
f3f02b89-25a6-4831-98ed-afbc6d0b49a8

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
DRE Dilator, Vessel, For Percutaneous Catheterization

GMDN Terms

Code Name
38128 Vascular dilator, single-use

Identifiers

Type ID
Unit of Use 07290019371007
Primary 37290019371008

Premarket Submissions

Submission Number Supplement Number
K211679 000