← Back to catalogue

Straight nasal tampon (exp.)

FDA UDI

Class I (US FDA UDI)

by Spiggle & Theis Medizintechnik GmbH

Identity

Trade Name
Straight nasal tampon (exp.) FDA UDI
Generic Name
Intranasal splint, non-biodegradable FDA UDI
Device Name
with non-stick surface, 80 mm 20 pieces per box FDA UDI
Model / Reference
66110N FDA UDI
Description
with non-stick surface, 80 mm 20 pieces per box FDA UDI

Identifiers

Catalog Number
66110N FDA UDI
Primary DI / UDI-DI
04250676712233 FDA UDI
FDA Product Code
LYA FDA UDI
GMDN Term
Intranasal splint, non-biodegradable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4780 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: Intranasal splint, non-biodegradable

Straight nasal tampon (exp.) by Spiggle & Theis Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intranasal splint, non-biodegradable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI be7ad477-a666-45a8-9b2d-f16bb41ed0e2 35 fields · synced May 31, 2026