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STILLE Clamps

FDA UDI

Class I (US FDA UDI)

by Stille AB

Identity

Trade Name
STILLE Clamps FDA UDI
Generic Name
Uterine tenaculum FDA UDI
Device Name
UTERINE MANIPULATOR STILLE probe 60 mm curved 26.5 cm 10.5 in FDA UDI
Model / Reference
107-13290 FDA UDI
Description
UTERINE MANIPULATOR STILLE probe 60 mm curved 26.5 cm 10.5 in FDA UDI

Identifiers

Catalog Number
107-13290 FDA UDI
Primary DI / UDI-DI
07332339210694 FDA UDI
FDA Product Code
GDJ FDA UDI
GMDN Term
Uterine tenaculum 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 — 26.5 Centimeter FDA UDI

Category: Uterine tenaculum

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

Similar devices

Also classified as Uterine tenaculum.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stille AB

Sources (1)

  • FDA UDI 3e33c9d6-3717-432c-85e0-d922ee5b6897 36 fields · synced Jun 1, 2026