Defender, Pair

FDA UDI

Class II (US FDA UDI)

by Precision Medical Products

Identity

Trade Name: Defender, Pair FDA UDI
Generic Name: Intermittent venous compression system FDA UDI
Model / Reference: 08-0028 FDA UDI

Identifiers

Primary DI / UDI-DI: 00194832000052 FDA UDI
510(k) Number: K212731 FDA UDI
FDA Product Code: JOW FDA UDI
GMDN Term: Intermittent venous compression system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.5800 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

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Intermittent venous compression system

Defender, Pair by Precision Medical Products — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K212731 also covers:

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: Precision Medical Products

Sources (1)

FDA UDI 9aabedde-7134-47f4-ac76-a8b2922d0754 33 fields · synced May 30, 2026