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Solvent Medical

FDA UDI

Class II (US FDA UDI)

by Solvent Medical

Identity

Trade Name
Solvent Medical FDA UDI
Generic Name
Electrocardiographic lead/catheter adaptor FDA UDI
Device Name
Disposable Temporary Pacing Cable FDA UDI
Model / Reference
649 FDA UDI
Description
Disposable Temporary Pacing Cable FDA UDI

Identifiers

Primary DI / UDI-DI
00862412000203 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

Yes

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

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Electrocardiographic lead/catheter adaptor

Solvent Medical by Solvent Medical — 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

Manufacturer
Solvent Medical

Sources (1)

  • FDA UDI 8599a476-7a22-4489-bc25-04be0c7dcc2b 34 fields · synced May 31, 2026