← Back to catalogue

DVT Sleeve

FDA UDI

Class II (US FDA UDI)

by Renu Medical, Inc

Identity

Trade Name
DVT Sleeve FDA UDI
Generic Name
Multi-chamber venous compression system garment, reprocessed FDA UDI
Device Name
Sequential thigh garment fits up to 35 in thigh circumference FDA UDI
Model / Reference
RM-TRP 40 FDA UDI
Description
Sequential thigh garment fits up to 35 in thigh circumference FDA UDI

Identifiers

Primary DI / UDI-DI
00816317023164 FDA UDI
510(k) Number
K031559 FDA UDI
FDA Product Code
JOW FDA UDI
GMDN Term
Multi-chamber venous compression system garment, reprocessed 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multi-chamber venous compression system garment, reprocessed

DVT Sleeve by Renu Medical, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-chamber venous compression system garment, reprocessed.

Cleared under the same submission

K031559 also covers:

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
Renu Medical, Inc

Sources (1)

  • FDA UDI 595e68fd-84a4-4b27-bc9d-f5765ca133a0 34 fields · synced Jun 8, 2026