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Sequential Circulator

FDA UDI

Class II (US FDA UDI)

by Bio Compression Systems, Inc.

Identity

Trade Name
Sequential Circulator FDA UDI
Generic Name
Sequential venous compression system inflator FDA UDI
Model / Reference
SC-3008-T-230 FDA UDI

Identifiers

Primary DI / UDI-DI
00812311021373 FDA UDI
510(k) Number
K043423 FDA UDI
FDA Product Code
JOW FDA UDI
GMDN Term
Sequential venous compression system inflator 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

No

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: Sequential venous compression system inflator

Sequential Circulator by Bio Compression Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sequential venous compression system inflator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f692e3f2-b282-4911-90e6-a496ce14aa6c 33 fields · synced May 30, 2026