FDA UDI In Commercial Distribution 🇺🇸 United States

DeRoyal

DI: 00749756120319 · Model: 89-5005 · DEROYAL INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
DeRoyal
Primary DI
00749756120319
Version / Model
89-5005
Catalog Number
89-5005
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
2
Public Version Date
2022-06-17
Public Version Status
Update
Public Device Record Key
3a72bed8-2474-403f-9ea6-9e82f13a5527

Device Description

STANDARD BASIN SET

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
33961 General surgical procedure kit, non-medicated, single-use

Identifiers

Type ID
Package 50749756120314
Primary 00749756120319

Customer Contacts