FDA UDI In Commercial Distribution 🇺🇸 United States

Premium Plus

DI: D8388122 · Model: 812 · Premium Plus International Limited
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

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Basic Information

Brand Name
Premium Plus
Primary DI
D8388122
Version / Model
812
Company Name
Premium Plus International Limited
Labeler DUNS
668367758
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2020-01-07
Public Version
1
Public Version Date
2020-01-15
Public Version Status
New
Public Device Record Key
17965b63-2452-4461-98ab-df0dbba03bbb

Device Description

Disposable Endo Sponges

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
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NAB Gauze / Sponge,Nonresorbable For External Use

GMDN Terms

Code Name
48130 Non-woven gauze pad, non-sterile

Identifiers

Type ID
Package D8388128
Primary D8388122
Unit of Use D8388120