← Back to catalogue

H3R Holster

FDA UDI

Class II (US FDA UDI)

by Tz Medical, Inc.

Identity

Trade Name
H3R Holster FDA UDI
Generic Name
Electrocardiographic ambulatory recorder FDA UDI
Device Name
H3R Holster (Rev A) FDA UDI
Model / Reference
H3R-0027 FDA UDI
Description
H3R Holster (Rev A) FDA UDI

Identifiers

Primary DI / UDI-DI
00811331013931 FDA UDI
510(k) Number
K102507 FDA UDI
FDA Product Code
DSI FDA UDI
GMDN Term
Electrocardiographic ambulatory recorder FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1025 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrocardiographic ambulatory recorder

H3R Holster by Tz Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic ambulatory recorder.

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

Manufacturer
Tz Medical, Inc.

Sources (1)

  • FDA UDI c3fd7e35-72b2-4c38-90f0-574063220bb5 34 fields · synced Jun 1, 2026