FDA UDI In Commercial Distribution 🇺🇸 United States

DeRoyal

DI: 00749756780971 · Model: NP-1002 · 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
00749756780971
Version / Model
NP-1002
Company Name
DEROYAL INDUSTRIES, INC.
Labeler DUNS
096372255
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-06-04
Public Version
2
Public Version Date
2021-08-10
Public Version Status
Update
Public Device Record Key
ef1ad3f7-07d3-474d-8ebf-dfcbea3a758e

Device Description

PRO-III Patient Tube & Filter

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
No
Sterilization Prior Use
No

Product Codes

Code Name
KDQ BOTTLE, COLLECTION, VACUUM

GMDN Terms

Code Name
47409 Negative-pressure wound therapy tubing set

Identifiers

Type ID
Package 50749756780976
Primary 00749756780971

Customer Contacts