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M-Ttl

FDA UDI

Class I (US FDA UDI)

by Quality Aspirators, Inc.

Identity

Trade Name
M-TTL FDA UDI
Generic Name
Head-worn lamp FDA UDI
Device Name
M-TTL FDA UDI
Model / Reference
M-TTL FDA UDI
Description
M-TTL FDA UDI

Identifiers

Catalog Number
317-10029 FDA UDI
Primary DI / UDI-DI
00814005024462 FDA UDI
FDA Product Code
KYT FDA UDI
GMDN Term
Head-worn lamp FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6350 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Head-worn lamp

M-Ttl by Quality Aspirators, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Head-worn lamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7e0ba134-6766-4255-bc04-91cc44b213f8 34 fields · synced Jun 8, 2026