FDA UDI In Commercial Distribution 🇺🇸 United States

IMCO

DI: 00815842021386 · Model: 2030-IMC · BIOPROTECH INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
IMCO
Primary DI
00815842021386
Version / Model
2030-IMC
Company Name
BIOPROTECH INC.
Labeler DUNS
688460539
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-05-16
Public Version
1
Public Version Date
2025-05-26
Public Version Status
New
Public Device Record Key
9e7d4a38-b5a9-4822-ad51-7c7f2a9b4796

Device Description

23x34(mm), PET+Ag/Agcl, Electrode, EKG TAB Resting

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DRX Electrode, Electrocardiograph

GMDN Terms

Code Name
35035 Electrocardiographic electrode, single-use

Identifiers

Type ID
Package 10815842021383
Primary 00815842021386
Package 30815842021387

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 40 Degrees Celsius