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Laser laryngoscope, size 6, black, for

FDA UDI

Class I (US FDA UDI)

by Spiggle & Theis Medizintechnik GmbH

Identity

Trade Name
Laser laryngoscope, size 6, black, for FDA UDI
Generic Name
Rigid bladed intubation laryngoscope, direct, reusable FDA UDI
Device Name
anterior commissure, length 182 mm ID 18x13 mm, OD 26x17 mm FDA UDI
Model / Reference
50-215-06 FDA UDI
Description
anterior commissure, length 182 mm ID 18x13 mm, OD 26x17 mm FDA UDI

Identifiers

Catalog Number
50-215-06 FDA UDI
Primary DI / UDI-DI
04250381858486 FDA UDI
FDA Product Code
CCW FDA UDI
GMDN Term
Rigid bladed intubation laryngoscope, direct, 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rigid bladed intubation laryngoscope, direct, reusable

Laser laryngoscope, size 6, black, for by Spiggle & Theis Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid bladed intubation laryngoscope, direct, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spiggle & Theis Medizintechnik GmbH

Sources (1)

  • FDA UDI e030008e-4005-47c8-aeaf-86dfba886d99 35 fields · synced Jun 1, 2026