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Ic-1200-Wh

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref IC-1200-WH

by Bio Compression Systems, Inc.

Identity

Trade Name
VascuEase FDA UDI
Generic Name
Sequential venous compression system inflator FDA UDI
Model / Reference
IC-1200-WH EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
00812311022011 EUDAMEDFDA UDI
Basic UDI-DI
B-00812311022011 EUDAMED
510(k) Number
K180248 FDA UDI
FDA Product Code
JOW FDA UDI
EMDN Code
Z120607 PNEUMATIC COMPRESSION EQUIPMENT EUDAMED
GMDN Term
Sequential venous compression system inflator FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
870.5800 FDA UDI
Market of Registration
Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Ic-1200-Wh by Bio Compression Systems, Inc. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000008442
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 7fa5a562-8cbd-42ff-b3c3-465efbccc7f1 61 fields · synced Aug 1, 2026
  • FDA UDI 307b70f3-5924-4a84-a1e3-a8a5e8a2d5c5 33 fields · synced May 30, 2026