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AbbVie Lightweight Vest L

FDA UDI

Class I (US FDA UDI)

by Abbvie Inc.

Identity

Trade Name
AbbVie Lightweight Vest L FDA UDI
Generic Name
Personal device holder, reusable FDA UDI
Device Name
The Lightweight Vest is designed to carry a CADD-Legacy® 1400 pump. This Lightweight Vest is intended for single-patient use only. FDA UDI
Model / Reference
10634 FDA UDI
Description
The Lightweight Vest is designed to carry a CADD-Legacy® 1400 pump. This Lightweight Vest is intended for single-patient use only. FDA UDI

Identifiers

Primary DI / UDI-DI
08054083008202 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 Lightweight Vest L 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 cb2892e9-0dbf-4e01-b3f4-c338f9604aee 33 fields · synced May 30, 2026