FDA UDI In Commercial Distribution 🇺🇸 United States

40643 Reverse Trendelenburg Kit - Universal

DI: 00787551038804 · Model: 40643 · XODUS MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
40643 Reverse Trendelenburg Kit - Universal
Primary DI
00787551038804
Version / Model
40643
Catalog Number
40643
Company Name
XODUS MEDICAL, INC.
Labeler DUNS
868042664
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-08
Public Version
1
Public Version Date
2022-12-16
Public Version Status
New
Public Device Record Key
9bb1a8f4-711f-449b-a6be-498972a2d1fe

Device Description

40643 Reverse Trendelenburg Kit - Universal

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
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
CCX SUPPORT, PATIENT POSITION

GMDN Terms

Code Name
65178 Operating table patient positioning set, single-use

Identifiers

Type ID
Package 20787551038808
Primary 00787551038804

Customer Contacts