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Kocher director

FDA UDI

Class I (US FDA UDI)

by Spiggle & Theis Medizintechnik GmbH

Identity

Trade Name
Kocher director FDA UDI
Generic Name
ENT probe, reusable FDA UDI
Device Name
with opening 12.5 mm, 16.5 cm FDA UDI
Model / Reference
80-470-16 FDA UDI
Description
with opening 12.5 mm, 16.5 cm FDA UDI

Identifiers

Catalog Number
80-470-16 FDA UDI
Primary DI / UDI-DI
04250676712998 FDA UDI
FDA Product Code
LRC FDA UDI
GMDN Term
ENT probe, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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: ENT probe, reusable

Kocher director by Spiggle & Theis Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ENT probe, 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 ac41caef-5eb5-4c34-bb74-7fe78d0b4436 35 fields · synced May 31, 2026