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AbbVie Chest Pack

FDA UDI

Class I (US FDA UDI)

by Abbvie Inc.

Identity

Trade Name
AbbVie Chest Pack FDA UDI
Generic Name
Personal device holder, reusable FDA UDI
Device Name
The Chest Pack is designed to carry a CADD-Legacy® 1400 pump. This Chest Pack is intended for single-patient use only. The Chest Pack is intended to be put on over the head and fastened around the chest. FDA UDI
Model / Reference
10635 FDA UDI
Description
The Chest Pack is designed to carry a CADD-Legacy® 1400 pump. This Chest Pack is intended for single-patient use only. The Chest Pack is intended to be put on over the head and fastened around the chest. FDA UDI

Identifiers

Primary DI / UDI-DI
08054083008103 FDA UDI
FDA Product Code
IQG FDA UDI
GMDN Term
Personal device holder, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5050 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

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Personal device holder, reusable

AbbVie Chest Pack by Abbvie Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Personal device holder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Abbvie Inc.

Sources (1)

  • FDA UDI 7990281d-7a13-4739-8517-6e3d5cba8b9c 33 fields · synced Jun 6, 2026