FDA UDI In Commercial Distribution 🇺🇸 United States

DeRoyal

DI: 00749756916004 · Model: 35-401068 · 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
00749756916004
Version / Model
35-401068
Catalog Number
35-401068
Company Name
DEROYAL INDUSTRIES, INC.
Labeler DUNS
096372255
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-08-23
Public Version
1
Public Version Date
2021-08-31
Public Version Status
New
Public Device Record Key
083b28cf-02fa-4fd7-896e-69c003de9c3d

Device Description

MEDLINE 2 PORT MANIFOLD W/ 10 in EXTENSION TBG

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DXT Injector and syringe, angiographic

GMDN Terms

Code Name
16545 Angiography kit

Identifiers

Type ID
Package 50749756916009
Primary 00749756916004

Customer Contacts