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LifeBand® Load-distributing Band

FDA UDI

Class II (US FDA UDI)

by ZOLL Circulation, Inc.

Identity

Trade Name
LifeBand® Load-distributing Band FDA UDI
Generic Name
Cardiac resuscitator band FDA UDI
Device Name
Single-use chest compression band. (3 per package) FDA UDI
Model / Reference
100 FDA UDI
Description
Single-use chest compression band. (3 per package) FDA UDI

Identifiers

Catalog Number
8700-0706-27 FDA UDI
Primary DI / UDI-DI
10849111001790 FDA UDI
510(k) Number
K112998 FDA UDI
FDA Product Code
DRM FDA UDI
GMDN Term
Cardiac resuscitator band FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cardiac resuscitator band

LifeBand® Load-distributing Band by ZOLL Circulation, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiac resuscitator band.

Cleared under the same submission

K112998 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
ZOLL Circulation, Inc.

Sources (1)

  • FDA UDI 0bcce038-2a50-43a2-9efc-f88410630f40 36 fields · synced Jun 9, 2026