← Back to catalogue

Wallace

FDA UDI

Class II (US FDA UDI)

by Icu Medical, Inc.

Identity

Trade Name
Wallace FDA UDI
Generic Name
Mechanical pipette FDA UDI
Model / Reference
WIC-45H-20 FDA UDI

Identifiers

Primary DI / UDI-DI
15019315081767 FDA UDI
FDA Product Code
MQH FDA UDI
GMDN Term
Mechanical pipette FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.6130 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Mechanical pipette

A comprehensive medical device directory entry for the Wallace, a manually-operated device used in Obstetrics/Gynecology for assisted reproduction.

Similar devices

Also classified as Mechanical pipette.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Icu Medical, Inc.

Sources (1)

  • FDA UDI c2bfd2a0-9eaf-4197-b647-db51f271f95c 32 fields · synced Aug 4, 2026