Laryngoscope Blade Set Mac 1, 2, 4 Miller 1, 2, 4 Medium Handle

FDA UDI

by Maco International

Identity

Trade Name: Laryngoscope Blade Set Mac 1,2,4 Miller 1,2,4 Medium Handle FDA UDI
Generic Name: Laryngoscope blade, reusable FDA UDI
Model / Reference: 3115 FDA UDI

Identifiers

Catalog Number: 3115 FDA UDI
Primary DI / UDI-DI: G27231150 FDA UDI
GMDN Term: Laryngoscope blade, reusable FDA UDI

Classification

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

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Laryngoscope blade, reusable Laryngoscope handle, reusable

Laryngoscope Blade Set Mac 1, 2, 4 Miller 1, 2, 4 Medium Handle by Maco International — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laryngoscope handle, reusable.

Surgical Direct — SURGICAL DIRECT, INC. · Class I
Surgical Direct — SURGICAL DIRECT, INC. · Class I
GreenLight™ — Airlife, Inc. · Class I
PILLING — TELEFLEX INCORPORATED · Class I
PILLING — TELEFLEX INCORPORATED · Class I
PILLING — TELEFLEX INCORPORATED · Class I
Surgical Direct — SURGICAL DIRECT, INC. · Class I
Surgical Direct — SURGICAL DIRECT, INC. · 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	N/A	Pending data

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

Manufacturer

Manufacturer: Maco International

Sources (1)

FDA UDI 675a875d-0127-4c68-8987-fc7869c70ffa 33 fields · synced Jun 6, 2026