← Back to catalogue

Sure-Lock

FDA UDI

Class II (US FDA UDI)

by Curbell Medical Products, Inc.

Identity

Trade Name
SURE-LOCK FDA UDI
Generic Name
Electrocardiographic electrode connector FDA UDI
Device Name
SURE LOCK,A34,10 PK,ORANGE LEVER,CURBELL BAG,TELIC LABEL FDA UDI
Model / Reference
SLC-4107-410 FDA UDI
Description
SURE LOCK,A34,10 PK,ORANGE LEVER,CURBELL BAG,TELIC LABEL FDA UDI

Identifiers

Catalog Number
22666 FDA UDI
Primary DI / UDI-DI
00840828161978 FDA UDI
510(k) Number
K080605 FDA UDI
FDA Product Code
DSA FDA UDI
GMDN Term
Electrocardiographic electrode connector 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 connector

Sure-Lock by Curbell Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic electrode connector.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 0c0bd4f3-f0cd-4013-8819-01faabdbd7b1 36 fields · synced Jun 1, 2026