← Back to catalogue

STILLE Retractors

FDA UDI

Class I (US FDA UDI)

by Stille AB

Identity

Trade Name
STILLE Retractors FDA UDI
Generic Name
Nasal speculum, reusable FDA UDI
Device Name
NASAL SPECULUM VIENNA STILLE 34 mm 14 cm 5.5 in FDA UDI
Model / Reference
108-27011-3 FDA UDI
Description
NASAL SPECULUM VIENNA STILLE 34 mm 14 cm 5.5 in FDA UDI

Identifiers

Catalog Number
108-27011-3 FDA UDI
Primary DI / UDI-DI
07332339212315 FDA UDI
FDA Product Code
EPY FDA UDI
GMDN Term
Nasal speculum, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.1800 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 — 14 Centimeter FDA UDI

Category: Nasal speculum, reusable

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

Similar devices

Also classified as Nasal speculum, reusable.

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

Manufacturer
Stille AB

Sources (1)

  • FDA UDI 06fe22be-d1a9-44dd-85fb-b1a62d978cc5 36 fields · synced May 30, 2026