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Pad 1115z

FDA UDI

Class II (US FDA UDI)

by Tz Medical, Inc.

Identity

Trade Name
PAD 1115Z FDA UDI
Generic Name
External defibrillation electrode, adult, reusable FDA UDI
Device Name
PADTACZ1 SERIES EXTENSION FDA UDI
Model / Reference
PAD 1115Z FDA UDI
Description
PADTACZ1 SERIES EXTENSION FDA UDI

Identifiers

Primary DI / UDI-DI
00811331017861 FDA UDI
510(k) Number
K983196 FDA UDI
FDA Product Code
DRO FDA UDI
GMDN Term
External defibrillation electrode, adult, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5550 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: External defibrillation electrode, adult, reusable

Pad 1115z by Tz Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External defibrillation electrode, adult, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tz Medical, Inc.

Sources (1)

  • FDA UDI 82898be7-aa1e-45b8-b8b9-4261330ccc56 34 fields · synced Jun 1, 2026