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Insighter

FDA UDI

Class I (US FDA UDI)

by Shenzhen Insighters Medical Technology Co., Ltd.

Identity

Trade Name
Insighter FDA UDI
Generic Name
Laryngeal mask airway, single-use FDA UDI
Model / Reference
iS-LMA-A 40 FDA UDI

Identifiers

Primary DI / UDI-DI
06970831725936 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

Yes

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

No

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

Yes

FDA UDI

Category: Laryngeal mask airway, single-use

Insighter by Shenzhen Insighters Medical Technology Co., Ltd. — 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 7e98ff68-8d95-4592-b1d9-b3a64276eec3 32 fields · synced Jun 1, 2026