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IntuBrite Sterile

FDA UDI

Class I (US FDA UDI)

by Salter Labs

Identity

Trade Name
IntuBrite Sterile FDA UDI
Generic Name
Laryngoscope blade, single-use FDA UDI
Device Name
MILLER 2/PEDIATRIC SINGLE USE DISPOSABLE LARYNGOSCOPE SYSTEM-STERILE FDA UDI
Model / Reference
S01-1032.C.2016.C FDA UDI
Description
MILLER 2/PEDIATRIC SINGLE USE DISPOSABLE LARYNGOSCOPE SYSTEM-STERILE FDA UDI

Identifiers

Catalog Number
S01-1032.C.2016.C FDA UDI
Primary DI / UDI-DI
00607411967962 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

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

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: Laryngoscope blade, single-use

IntuBrite Sterile by Salter Labs — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laryngoscope blade, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Salter Labs

Sources (1)

  • FDA UDI b2d6daa5-539c-4951-8a0e-0255b0ec460a 35 fields · synced Jun 1, 2026