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Equipment box for external nasal splints

FDA UDI

Class I (US FDA UDI)

by Spiggle & Theis Medizintechnik GmbH

Identity

Trade Name
Equipment box for external nasal splints FDA UDI
Generic Name
External nasal splint FDA UDI
Device Name
1 Box FDA UDI
Model / Reference
2060500 FDA UDI
Description
1 Box FDA UDI

Identifiers

Catalog Number
2060500 FDA UDI
Primary DI / UDI-DI
04250381856338 FDA UDI
FDA Product Code
EPP FDA UDI
GMDN Term
External nasal splint FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.5800 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

Category: External nasal splint

Equipment box for external nasal splints by Spiggle & Theis Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External nasal splint.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7755ed42-62a0-4bbc-993c-ce01d2a9a3f6 35 fields · synced May 30, 2026