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Curaplex

FDA UDI

Class I (US FDA UDI)

by Bound Tree Medical, Llc

Identity

Trade Name
Curaplex FDA UDI
Generic Name
Laryngeal mask airway, single-use FDA UDI
Device Name
Airway Supraglottic LTS-D #4 Kit W/ET Holder FDA UDI
Model / Reference
KLTSD404K FDA UDI
Description
Airway Supraglottic LTS-D #4 Kit W/ET Holder FDA UDI

Identifiers

Catalog Number
KLTSD404K FDA UDI
Primary DI / UDI-DI
00812277033700 FDA UDI
FDA Product Code
CAE FDA UDI
GMDN Term
Laryngeal mask airway, 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Laryngeal mask airway, single-use

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

Similar devices

Also classified as Laryngeal mask airway, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 04c3ea5c-872e-460a-bf59-16b83df4ef70 34 fields · synced Jun 1, 2026