FDA UDI In Commercial Distribution 🇺🇸 United States

DeRoyal

DI: 00749756960281 · Model: 89-9963 · DEROYAL INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
DeRoyal
Primary DI
00749756960281
Version / Model
89-9963
Catalog Number
89-9963
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
d7902512-e2b9-4fcb-a1b6-6cbfa7652b52

Device Description

ANGIOGRAPHY 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 50749756960286
Primary 00749756960281

Customer Contacts