LEAD WIRE,PINCH TO NIHON KONDEN,INTERMED

Primary DI
90840828101519
Brand
LEAD WIRE,PINCH TO NIHON KONDEN,INTERMED
Company
CURBELL MEDICAL PRODUCTS, INC.
Model
DLW-06BF-MXAN-3000
Catalog number
18604
Device description
LEAD WIRE,PINCH TO NIHON KONDEN,INTERMED
Published
2016-09-24
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
MR Unsafe
Rx
true
OTC
false
Sterile
false
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
DSACable, Transducer And Electrode, Patient, (Including Connector)

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DSACable, Transducer And Electrode, Patient, (Including Connector)Cardiovascular2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
90840828101199PackageGS110Not in Commercial Distribution
90840828101519PackageGS12Not in Commercial Distribution
90840828101045PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
9084082810119990840828101199
9084082810151990840828101519
9084082810104590840828101045

GMDN Terms#

Term, Definition table
TermDefinition
Electrocardiographic electrode, single-useA non-sterile, noninvasive electrical conductor designed to conduct electrical signals, generated by a patient's heart, from the skin surface to an electrocardiograph (ECG) monitoring device, via an ECG lead wire (not included). It is typically a disk-like electrode that is affixed to the skin with a special adhesive, adhesive tape, or suction mechanism; a conductive gel may be pre-applied and it may include a skin cleaning wipe to assist electrical connection. Electrocardiography is usually performed using a set of electrodes (e.g., 10) connected to appropriate leads and cables. This is a single-use device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
1-800-235-7500mwinter@curbellmedical.com

Regulatory Flags#

DUNS number
796452311
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
false
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00840828196444GEN4 INTERACTIVE421384U-0709008307402026-05-19
00840828196451GEN4 PLUS, DIRECT ACCESS5C050U-P10000288307442026-05-19
00840828196406GEN4 INTERACTIVE42119CU-0104018307102026-05-07
00840828196413GEN4 PLUS, DIRECT ACCESS5C330U-Z10300011307092026-05-07
00840828196420800 S37,JE,BE,2L,790,BE ON 6&8BIC-19C0-A08-8307022026-05-07
00840828196437GEN4 INTERACTIVE437370U-0119728307152026-05-07
00840828196369GEN4 INTERACTIVE45331E-S14059F306952026-04-23
00840828196376GEN4 INTERACTIVE43719FU-0103018307002026-04-23
00840828196383GEN4 PLUS, DIRECT ACCESS5C430U-Z3020000F307012026-04-23
00840828196390GEN4 PLUS, DIRECT ACCESS5C422U-Z12700028307062026-04-23
00840828196338CALLCD,800,180,NO LOGO,WIRED FOR CACC180-986306882026-04-14
00840828196345RESPONDER 5, INTERACTIVE5I41JU-562427A306892026-04-14
00840828196352RESPONDER 5, INTERACTIVE5I41UU-801002A306922026-04-14
00840828196321SURELOCK, CURBELL/PHILIPS, BLUE, 10 PK989803209691306232026-04-09
00840828196284GEN4 INTERACTIVE410370E-0104468306862026-04-08
00840828196291BED COVER-4X36X88-CEN PRO PLUS MAT TOP-PBMC-43688-CENPROPLUSTOP-PC306852026-04-08
00840828196246RESPONDER 5, INTERACTIVE5I414U-164031A306742026-04-01
00840828196253GEN4 INTERACTIVE45422U-S103028306802026-04-01
00840828196260GEN4 PLUS, DIRECT ACCESS5C19DU-Z15900178306762026-04-01
00840828196277GEN4 INTERACTIVE425331U-0150518306512026-04-01

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