← Back to catalogue

Cmi

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 444FC

by Utah Medical Products, Inc.

Identity

Trade Name
Flex Cup EUDAMED
CMI FDA UDI
Generic Name
Foetal vacuum extraction system cup, single-use FDA UDI
Device Name
CMI Vacuum Delivery Cups EUDAMED
OBSTETRICAL VACUUM DELIVERY KIT, 60mm Flex Cup, Tube, & Fluid Trap FDA UDI
Model / Reference
444FC EUDAMED
Flex Cup FDA UDI
Description
OBSTETRICAL VACUUM DELIVERY KIT, 60mm Flex Cup, Tube, & Fluid Trap FDA UDI

Identifiers

Catalog Number
444FC FDA UDI
Primary DI / UDI-DI
H671444FC0 EUDAMEDFDA UDI
Basic UDI-DI
++H671CE012IIAC4 EUDAMED
510(k) Number
K910788 FDA UDI
FDA Product Code
HIS FDA UDI
EMDN Code
Z12080301 OBSTETRIC VACUUM EXTRACTORS EUDAMED
GMDN Term
Foetal vacuum extraction system cup, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
884.5300 FDA UDI
Market of Registration
Ireland EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — 60 Millimeter FDA UDI

Category: Foetal vacuum extraction system cup, single-use

Cmi by Utah Medical Products, Inc. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Foetal vacuum extraction system cup, single-use.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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

Manufacturer

Sources (2)

  • FDA UDI 2141770c-538a-4f7c-92ec-6f89f1ffa97f 37 fields · synced Jun 19, 2026
  • EUDAMED 608b0ba4-def0-442f-9999-526635ee458b 61 fields · synced Jun 19, 2026