FDA UDI In Commercial Distribution 🇺🇸 United States

DeRoyal

DI: 00749756977920 · Model: 89-10022 · DEROYAL INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
DeRoyal
Primary DI
00749756977920
Version / Model
89-10022
Catalog Number
89-10022
Company Name
DEROYAL INDUSTRIES, INC.
Labeler DUNS
096372255
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-05-07
Public Version
1
Public Version Date
2021-05-17
Public Version Status
New
Public Device Record Key
164374be-e41b-408a-8159-f6a28f80bf3e

Device Description

INTL-CATH LAB PACK

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
OEQ Angiography/angioplasty kit

GMDN Terms

Code Name
16545 Angiography kit

Identifiers

Type ID
Package 50749756977925
Primary 00749756977920

Customer Contacts