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STILLE Various Instruments

FDA UDI

Class I (US FDA UDI)

by Stille AB

Identity

Trade Name
STILLE Various Instruments FDA UDI
Generic Name
Cast/plaster saw FDA UDI
Device Name
SOFT PROFILES for PLASTER CAST REMOVER STILLE 100 pcs 85 cm 33.5 in FDA UDI
Model / Reference
413-2504-85 FDA UDI
Description
SOFT PROFILES for PLASTER CAST REMOVER STILLE 100 pcs 85 cm 33.5 in FDA UDI

Identifiers

Catalog Number
413-2504-85 FDA UDI
Primary DI / UDI-DI
07332339210496 FDA UDI
FDA Product Code
LGG FDA UDI
GMDN Term
Cast/plaster saw FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.5980 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

Dimensions & Sizes

Size
Length — 85 Centimeter FDA UDI

Category: Cast/plaster saw

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

Similar devices

Also classified as Cast/plaster saw.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stille AB

Sources (1)

  • FDA UDI 44928baa-81f0-493b-a142-fdb57fa7e246 36 fields · synced May 31, 2026