FORWARD Finger Thoracostomy Kit - Bilateral

FDA UDI

Class I (US FDA UDI)

by Integrated Medcraft Llc

Identity

Trade Name: FORWARD Finger Thoracostomy Kit - Bilateral FDA UDI
Generic Name: Pneumothorax catheter insertion set FDA UDI
Device Name: Convenience kit for bilateral finger thoracostomy procedure, including items for skin prep, instruments, and chest seal. FDA UDI
Model / Reference: 4818-32501 FDA UDI
Description: Convenience kit for bilateral finger thoracostomy procedure, including items for skin prep, instruments, and chest seal. FDA UDI

Identifiers

Primary DI / UDI-DI: 00850056748476 FDA UDI
FDA Product Code: PYI FDA UDI
GMDN Term: Pneumothorax catheter insertion set FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4200 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pneumothorax catheter insertion set

FORWARD Finger Thoracostomy Kit - Bilateral by Integrated Medcraft Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Integrated Medcraft Llc

Sources (1)

FDA UDI 08976aa3-c97d-471b-a946-dc003439ab83 33 fields · synced Jun 8, 2026