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Pipette

FDA UDI

Class II (US FDA UDI)

by FIM Medical

Identity

Trade Name
Pipette FDA UDI
Generic Name
Breathing mouthpiece, single-use FDA UDI
Model / Reference
Pipette FDA UDI

Identifiers

Primary DI / UDI-DI
03760253450263 FDA UDI
510(k) Number
K080278 FDA UDI
FDA Product Code
CCJ FDA UDI
GMDN Term
Breathing mouthpiece, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1430 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Breathing mouthpiece, single-use

Pipette by FIM Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Breathing mouthpiece, single-use.

Cleared under the same submission

K080278 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
FIM Medical

Sources (1)

  • FDA UDI 773557f0-4ebb-4405-90bd-fc069c605da5 34 fields · synced May 30, 2026