FDA UDI In Commercial Distribution 🇺🇸 United States

PROPLATE

DI: 08809083941857 · Model: 9571C · BIOPROTECH INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
PROPLATE
Primary DI
08809083941857
Version / Model
9571C
Catalog Number
9571C
Company Name
BIOPROTECH INC.
Labeler DUNS
688460539
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-12
Public Version
2
Public Version Date
2020-06-05
Public Version Status
Update
Public Device Record Key
49d83b0e-94eb-4bee-85a4-161a0d205924

Device Description

Electrosurgical Unit Ground Pad, Disposable, Single use, Neutral electrode, Non-corded, Horizontal, Solid, Adult, 180x120mm

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
58494 Electrosurgical return electrode, single-use

Identifiers

Type ID
Package 28809083941851
Package 18809083941854
Primary 08809083941857

Premarket Submissions

Submission Number Supplement Number
K073360 000

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
-10 – 40 Degrees Celsius