FDA UDI In Commercial Distribution 🇺🇸 United States

Edwards

DI: 00690103218015 · Model: 10000CR · Edwards Lifesciences LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Edwards
Primary DI
00690103218015
Version / Model
10000CR
Catalog Number
10000CR
Company Name
Edwards Lifesciences LLC
Labeler DUNS
134139174
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-01-07
Public Version
2
Public Version Date
2025-06-30
Public Version Status
Update
Public Device Record Key
835acd73-37cb-4c8d-95b2-ec06e404856a

Device Description

Edwards Reusable Cradle

Device Characteristics

Single Use
No
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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
QWA Cardiovascular Delivery Catheter System Positioning And Stabilization Device

GMDN Terms

Code Name
63544 Cardiac implantation catheter platform base, single-use

Identifiers

Type ID
Primary 00690103218015

Customer Contacts

Storage Conditions

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