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Sklar®

FDA UDI

Class I (US FDA UDI)

by Sklar Corporation

Identity

Trade Name
Sklar® FDA UDI
Generic Name
Intrauterine curette, manual FDA UDI
Device Name
SCHRODER CURETTE #1 12" FDA UDI
Model / Reference
90-5461 FDA UDI
Description
SCHRODER CURETTE #1 12" FDA UDI

Identifiers

Primary DI / UDI-DI
10649111096310 FDA UDI
FDA Product Code
HCY FDA UDI
GMDN Term
Intrauterine curette, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.4530 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Intrauterine curette, manual

Sklar\u00f3 is a high-quality, hand-held surgical instrument designed for the removal of early or non-viable embryos/foetuses from the uterine lining during gynaecological procedures. This reusable device is made of high-grade stainless steel and features a sharp or blunt scraping tip, available in various shapes and sizes.

Similar devices

Also classified as Intrauterine curette, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sklar Corporation

Sources (1)

  • FDA UDI d34ad7f8-6426-43d1-9f46-68efac1f438e 33 fields · synced Jul 25, 2026