FDA UDI In Commercial Distribution 🇺🇸 United States

Maxtaping

DI: 00840270610369 · Model: 8080-BU-F · Oppo Medical Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
Maxtaping
Primary DI
00840270610369
Version / Model
8080-BU-F
Catalog Number
8080
Company Name
Oppo Medical Inc.
Labeler DUNS
830140807
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2025-04-01
Public Version
1
Public Version Date
2025-04-09
Public Version Status
New
Public Device Record Key
b765f2b8-1ef0-45ff-9fca-eb52fa52045e

Device Description

Maxtaping, 97mm Width x 151mm Length (5 Sheets/ Pack)

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KOX Solvent, Adhesive Tape

GMDN Terms

Code Name
10284 Pressure bandage, non-latex, single-use

Identifiers

Type ID
Unit of Use 00840270610529
Primary 00840270610369

Device Sizes

Type Value Unit Text
Length 15.1 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Please store this product at room temperature. Do not expose to excessive heat or moisture.