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Sjm™

FDA UDI

Class II (US FDA UDI)

by St. Jude Medical Cardiovascular Division

Identity

Trade Name
SJM™ FDA UDI
Generic Name
Electrocardiographic lead/catheter adaptor FDA UDI
Model / Reference
401760 FDA UDI

Identifiers

Catalog Number
401760 FDA UDI
Primary DI / UDI-DI
05414734053679 FDA UDI
FDA Product Code
DSA FDA UDI
GMDN Term
Electrocardiographic lead/catheter adaptor 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

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 2.4 Meter FDA UDI

Category: Electrocardiographic lead/catheter adaptor

Sjm™ by St. Jude Medical Cardiovascular Division — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic lead/catheter adaptor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5a11f28b-354b-4277-91a6-13df25aeb82c 36 fields · synced Jun 1, 2026