FDA UDI In Commercial Distribution 🇺🇸 United States

DeRoyal

DI: 00749756030274 · Model: 30-705 · DEROYAL INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
DeRoyal
Primary DI
00749756030274
Version / Model
30-705
Catalog Number
30-705
Company Name
DEROYAL INDUSTRIES, INC.
Labeler DUNS
096372255
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-30
Public Version
1
Public Version Date
2021-07-08
Public Version Status
New
Public Device Record Key
3b8e7b39-0236-4441-9220-f3dcee963d30

Device Description

Suture Boot

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KDC INSTRUMENT, SURGICAL, DISPOSABLE

GMDN Terms

Code Name
35257 Vascular booties

Identifiers

Type ID
Package 50749756030279
Primary 00749756030274
Package 30749756030275

Customer Contacts