Curaplex

FDA UDI

Class I (US FDA UDI)

by Bound Tree Medical, Llc

Identity

Trade Name: Curaplex FDA UDI
Generic Name: Laryngoscope blade, single-use FDA UDI
Device Name: Curaplex Select GreenLine/D Laryngoscope Blade, MILLER 1, Fiber Optic, Infant, Disposable 20ea/cs FDA UDI
Model / Reference: B-3110 FDA UDI
Description: Curaplex Select GreenLine/D Laryngoscope Blade, MILLER 1, Fiber Optic, Infant, Disposable 20ea/cs FDA UDI

Identifiers

Catalog Number: 301-B3110EA FDA UDI
Primary DI / UDI-DI: 00810071636820 FDA UDI
FDA Product Code: CCW FDA UDI
GMDN Term: Laryngoscope blade, single-use 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

Yes

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

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

Sterilization Method

Ethylene Oxide FDA UDI

Category: Laryngoscope blade, single-use

Curaplex by Bound Tree Medical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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IntuBrite Sterile — SALTER LABS · Class I
SunMed — SunMed · Class I
RUSCH — TELEFLEX INCORPORATED · Class I
Disposable Conventional Laryngoscope Blade — Maco International · 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

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Manufacturer

Manufacturer: Bound Tree Medical, Llc

Sources (1)

FDA UDI b86b97c5-1516-4d7b-880f-f4fcd5ca084d 34 fields · synced May 31, 2026