← Back to catalogue

AbbVie Hip Pack

FDA UDI

Class I (US FDA UDI)

by Abbvie Inc.

Identity

Trade Name
AbbVie Hip Pack FDA UDI
Generic Name
Personal device holder, reusable FDA UDI
Device Name
The Hip Pack is designed to carry a CADD-Legacy® 1400 pump. This Hip Pack is intended for single-patient use only. The Hip Pack is intended to be worn around the waist. FDA UDI
Model / Reference
10637 FDA UDI
Description
The Hip Pack is designed to carry a CADD-Legacy® 1400 pump. This Hip Pack is intended for single-patient use only. The Hip Pack is intended to be worn around the waist. FDA UDI

Identifiers

Primary DI / UDI-DI
08054083007953 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 Hip 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Abbvie Inc.

Sources (1)

  • FDA UDI d1246213-f28f-497c-8233-2fe5004e5d2d 33 fields · synced May 30, 2026