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Surelock, Midmark, Blue, 10 Pk

FDA UDI

Class II (US FDA UDI)

by Curbell Medical Products, Inc.

Identity

Trade Name
SURELOCK, MIDMARK, BLUE, 10 PK FDA UDI
Generic Name
Electrocardiographic electrode, reusable FDA UDI
Device Name
SURELOCK, MIDMARK, BLUE, 10 PK, SLC SERIES FDA UDI
Model / Reference
3-047-0005 FDA UDI
Description
SURELOCK, MIDMARK, BLUE, 10 PK, SLC SERIES FDA UDI

Identifiers

Catalog Number
28360 FDA UDI
Primary DI / UDI-DI
00840828188760 FDA UDI
510(k) Number
K080605 FDA UDI
FDA Product Code
DSA FDA UDI
GMDN Term
Electrocardiographic electrode, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2900 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Electrocardiographic electrode, reusable

Surelock, Midmark, Blue, 10 Pk by Curbell Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic electrode, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d4c5a972-f88d-4a3e-b20d-d5d924d5d3e0 36 fields · synced May 30, 2026