FDA UDI In Commercial Distribution 🇺🇸 United States

DeRoyal

DI: 00749756683449 · Model: 32-1850 · DEROYAL INDUSTRIES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
DeRoyal
Primary DI
00749756683449
Version / Model
32-1850
Catalog Number
32-1850
Company Name
DEROYAL INDUSTRIES, INC.
Labeler DUNS
096372255
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-28
Public Version
1
Public Version Date
2021-08-05
Public Version Status
New
Public Device Record Key
48ce33a1-5b9b-411e-a899-f2b8016f9bd9

Device Description

ST. 7 In Knee Roll w/Cover

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NAB Gauze / sponge,nonresorbable for external use

GMDN Terms

Code Name
46854 Wound-nonadherent dressing, absorbent, non-antimicrobial

Identifiers

Type ID
Package 50749756683444
Primary 00749756683449

Customer Contacts