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STILLE Rasps

FDA UDI

Class I (US FDA UDI)

by Stille AB

Identity

Trade Name
STILLE Rasps FDA UDI
Generic Name
Nasal file/rasp FDA UDI
Device Name
RASP FOMON STILLE double-ended TC-inserts 5&6 21.5 cm 8.5 in FDA UDI
Model / Reference
111-22862 FDA UDI
Description
RASP FOMON STILLE double-ended TC-inserts 5&6 21.5 cm 8.5 in FDA UDI

Identifiers

Catalog Number
111-22862 FDA UDI
Primary DI / UDI-DI
07332339212124 FDA UDI
FDA Product Code
HTR FDA UDI
GMDN Term
Nasal file/rasp FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 21.5 Centimeter FDA UDI

Category: Nasal file/rasp

STILLE Rasps by Stille AB — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal file/rasp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stille AB

Sources (1)

  • FDA UDI d4710c13-bc9d-462f-a978-9a4a7b069f93 36 fields · synced May 30, 2026