PROACT Smoothline LF

FDA UDI

Class I (US FDA UDI)

by Proact Medical Limited

Identity

Trade Name: PROACT Smoothline LF FDA UDI
Generic Name: Laryngoscope blade, reusable FDA UDI
Device Name: Smoothline LF Green System Laryngoscope Blade, Autoclavable, Low Friction, Mac 5 FDA UDI
Model / Reference: SLGS30MAC5 FDA UDI
Description: Smoothline LF Green System Laryngoscope Blade, Autoclavable, Low Friction, Mac 5 FDA UDI

Identifiers

Catalog Number: SLGS30MAC5 FDA UDI
Primary DI / UDI-DI: 25056094502127 FDA UDI
FDA Product Code: CCW FDA UDI
GMDN Term: Laryngoscope blade, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.5540 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Laryngoscope blade, reusable

PROACT Smoothline LF by Proact Medical Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laryngoscope blade, reusable.

Xenamed Industries — Xenamed Industries · Class I
WL Economy Macintosh blade, no. 2, socle blue — Kirchner & Wilhelm GmbH + Co KG · Class I
Carnegie Surgical LLC — Carnegie Surgical LLC · Class I
Laryngoscope Lunalite 'D' Mac Blade No.4 — Medical Devices (Pvt) Ltd · Class I
Diamond Fibrelight Case / Blade (Seward Size 1, Macintosh Size 3, 4), Standard Handle — Penlon Limited · Class I
Reusable Conventional Blade Wisconsin 4 — FLEXICARE MEDICAL LIMITED · Class I
Heating Connector for Jet-Laryngoscopes with Mounting Points — CARL REINER GmbH Medizintechnik für Diagnose und Therapie Manufaktur chirurgischer Instrumente · Class IIa
Sklar® — Sklar Corporation · Class I

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

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

Manufacturer

Manufacturer: Proact Medical Limited

Sources (1)

FDA UDI 863a4f39-7334-4066-9723-a1c6d10ee155 36 fields · synced Jun 8, 2026