FDA UDI In Commercial Distribution 🇺🇸 United States

PROPEL

DI: 00763000710453 · Model: 60044- · MEDTRONIC XOMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
PROPEL
Primary DI
00763000710453
Version / Model
60044-
Company Name
MEDTRONIC XOMED, INC.
Labeler DUNS
835465063
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-08
Public Version
2
Public Version Date
2024-03-05
Public Version Status
Update
Public Device Record Key
669895b5-e3f6-4981-bde7-422698c776c2

Device Description

IMPLANT 60044- PROPEL MINI WITH SDS

Device Characteristics

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OWO Drug-eluting sinus stent

GMDN Terms

Code Name
61370 Drug-eluting paranasal sinus stent

Identifiers

Type ID
Package 20763000710464
Primary 00763000710453

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P100044 046

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius