Squid

FDA UDI

Class II (US FDA UDI)

by Portable Therapeutix

Identity

Trade Name: Squid FDA UDI
Generic Name: Inflatable hot/cold therapy pack/electric pump FDA UDI
Device Name: Squid - Circumferential Leg FDA UDI
Model / Reference: Circumferential Leg FDA UDI
Description: Squid - Circumferential Leg FDA UDI

Identifiers

Primary DI / UDI-DI: 00811107020644 FDA UDI
FDA Product Code: IRP FDA UDI
IME FDA UDI
GMDN Term: Inflatable hot/cold therapy pack/electric pump FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 890.5650 FDA UDI
890.5700 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Inflatable hot/cold therapy pack/electric pump

Squid by Portable Therapeutix — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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BREG — Breg, Inc. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Portable Therapeutix

Sources (1)

FDA UDI 42d0facf-27b1-4215-81c9-9f380a9d1a6d 33 fields · synced Jun 9, 2026