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FORWARD Oral Airway Kit

FDA UDI

Class I (US FDA UDI)

by Integrated Medcraft Llc

Identity

Trade Name
FORWARD Oral Airway Kit FDA UDI
Generic Name
Intrauterine cannula, single-use FDA UDI
Device Name
Oral Airway Kit that contains airway sizes 5, 6.5, 7, 8, 9, 10, and 12 FDA UDI
Model / Reference
1011-40002 FDA UDI
Description
Oral Airway Kit that contains airway sizes 5, 6.5, 7, 8, 9, 10, and 12 FDA UDI

Identifiers

Primary DI / UDI-DI
00850056748179 FDA UDI
FDA Product Code
CAE FDA UDI
GMDN Term
Intrauterine cannula, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5110 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

Yes

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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: Intrauterine cannula, single-use

FORWARD Oral Airway Kit by Integrated Medcraft Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intrauterine cannula, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e99305ee-11d0-4627-82c5-5293a02181a7 33 fields · synced May 30, 2026