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mouthpiece

FDA UDI

Class I (US FDA UDI)

by Sdi Diagnostics, Inc.

Identity

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

Identifiers

Catalog Number
F0360-200 FDA UDI
Primary DI / UDI-DI
B279F0360200 FDA UDI
FDA Product Code
BYP FDA UDI
GMDN Term
Breathing mouthpiece, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5620 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Breathing mouthpiece, single-use

mouthpiece by Sdi Diagnostics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Breathing mouthpiece, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9b4191d2-2374-4e07-82ed-715d22370518 33 fields · synced Jun 1, 2026