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bcI

FDA UDI

Class II (US FDA UDI)

by Icu Medical, Inc.

Identity

Trade Name
bcI FDA UDI
Generic Name
Intravenous pressure infusor, automated FDA UDI
Model / Reference
7204045 FDA UDI

Identifiers

Primary DI / UDI-DI
00695085800210 FDA UDI
FDA Product Code
KZL FDA UDI
GMDN Term
Intravenous pressure infusor, automated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9205 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

Yes

FDA UDI

Category: Intravenous pressure infusor, automated

bcI by Icu Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravenous pressure infusor, automated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Icu Medical, Inc.

Sources (1)

  • FDA UDI 7946f2f0-1454-4c5e-bc07-ce51fb419ba3 32 fields · synced May 30, 2026