FDA UDI In Commercial Distribution 🇺🇸 United States

DeRoyal

DI: 00749756962100 · Model: 32-2101 · DEROYAL INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
DeRoyal
Primary DI
00749756962100
Version / Model
32-2101
Catalog Number
32-2101
Company Name
DEROYAL INDUSTRIES, INC.
Labeler DUNS
096372255
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-12
Public Version
1
Public Version Date
2021-07-20
Public Version Status
New
Public Device Record Key
da003d7c-2b12-4f56-a1a0-3dd0cb363a11

Device Description

Custom Foam Brick

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KDD Kit, surgical instrument, disposable

GMDN Terms

Code Name
62292 Freestanding patient positioner, single-use

Identifiers

Type ID
Package 50749756962105
Primary 00749756962100

Customer Contacts