FDA UDI In Commercial Distribution 🇺🇸 United States

90920 Trendelenburg Pad XL

DI: 00787551037715 · Model: 90920 · XODUS MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
90920 Trendelenburg Pad XL
Primary DI
00787551037715
Version / Model
90920
Catalog Number
90920
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
94af30df-0116-4b94-9f96-17bfca97167f

Device Description

90920 Trendelenburg Pad XL

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
62789 Operating table non-slip back pad

Identifiers

Type ID
Package 20787551037719
Primary 00787551037715

Customer Contacts