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STILLE Titanium Micro Forceps

FDA UDI

Class I (US FDA UDI)

by Stille AB

Identity

Trade Name
STILLE Titanium Micro Forceps FDA UDI
Generic Name
Surgical soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Device Name
STILLE TI MICRO FORCEPS, Ring tips 1.0x0.5 mm, Diamond Jaws, Counter-balanced, Straight, 18 cm 7 in FDA UDI
Model / Reference
117-B140-18-TI FDA UDI
Description
STILLE TI MICRO FORCEPS, Ring tips 1.0x0.5 mm, Diamond Jaws, Counter-balanced, Straight, 18 cm 7 in FDA UDI

Identifiers

Catalog Number
117-B140-18-TI FDA UDI
Primary DI / UDI-DI
07332339222727 FDA UDI
FDA Product Code
GEN FDA UDI
GMDN Term
Surgical soft-tissue manipulation forceps, tweezers-like, reusable 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 — 18 Centimeter FDA UDI

Category: Surgical soft-tissue manipulation forceps, tweezers-like, reusable

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

Similar devices

Also classified as Surgical soft-tissue manipulation forceps, tweezers-like, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stille AB

Sources (1)

  • FDA UDI 1c543f5c-7ffb-44ed-bee6-62969466d96d 36 fields · synced May 30, 2026