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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
Endoscopic surgical probe FDA UDI
Device Name
PROBE STILLE blunt 19.5 cm 7.75 in FDA UDI
Model / Reference
119-10928-1 FDA UDI
Description
PROBE STILLE blunt 19.5 cm 7.75 in FDA UDI

Identifiers

Catalog Number
119-10928-1 FDA UDI
Primary DI / UDI-DI
07332339207694 FDA UDI
FDA Product Code
HXB FDA UDI
GMDN Term
Endoscopic surgical probe FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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 — 19.5 Centimeter FDA UDI

Category: Endoscopic surgical probe

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

Similar devices

Also classified as Endoscopic surgical probe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stille AB

Sources (1)

  • FDA UDI 245f7fba-2de5-48f0-86b1-49edce56ade2 36 fields · synced May 30, 2026