FDA UDI In Commercial Distribution 🇺🇸 United States

Edwards 23F Guide Sheath

DI: 00690103219784 · Model: 9880GS · Edwards Lifesciences LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Edwards 23F Guide Sheath
Primary DI
00690103219784
Version / Model
9880GS
Catalog Number
9880GSA
Company Name
Edwards Lifesciences LLC
Labeler DUNS
134139174
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-01-30
Public Version
1
Public Version Date
2026-02-09
Public Version Status
New
Public Device Record Key
ed7abbe5-ce95-4558-8723-0ed1bc8f1a42

Device Description

Edwards 23F Guide Sheath

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
NPU Prosthesis, Mitral Valve, Percutaneously Delivered

GMDN Terms

Code Name
58865 Vascular catheter introduction set, nonimplantable

Identifiers

Type ID
Primary 00690103219784

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P250019 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a cool, dry place