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Wisconsin LED Blade

FDA UDI

Class I (US FDA UDI)

by Maco International

Identity

Trade Name
Wisconsin LED Blade FDA UDI
Generic Name
Laryngoscope blade, reusable FDA UDI
Model / Reference
L8662-1 FDA UDI

Identifiers

Catalog Number
L8662-1 FDA UDI
Primary DI / UDI-DI
G272L866210 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Laryngoscope blade, reusable

Wisconsin LED Blade by Maco International — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laryngoscope blade, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Maco International

Sources (1)

  • FDA UDI dba88edc-dcdd-444a-822c-744e3459788a 33 fields · synced May 30, 2026