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Bio Compression Systems Multi-Flo DVT Model IC-1545-DLI

FDA UDI

Class II (US FDA UDI)

by Bio Compression Systems, Inc.

Identity

Trade Name
Bio Compression Systems Multi-Flo DVT Model IC-1545-DLI FDA UDI
Generic Name
Inflatable hot/cold therapy pack/electric pump FDA UDI
Model / Reference
IC-1545-DLI FDA UDI

Identifiers

Primary DI / UDI-DI
00812311022042 FDA UDI
510(k) Number
K131306 FDA UDI
FDA Product Code
JOW FDA UDI
GMDN Term
Inflatable hot/cold therapy pack/electric pump 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

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Inflatable hot/cold therapy pack/electric pumpIntermittent venous compression system pump

Bio Compression Systems Multi-Flo DVT Model IC-1545-DLI by Bio Compression Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Intermittent venous compression system pump.

Cleared under the same submission

K131306 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bio Compression Systems, Inc.

Sources (1)

  • FDA UDI 905a1d72-3098-46ec-8817-340ef247a49a 33 fields · synced May 30, 2026