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Gimmi

FDA UDI

Class I (US FDA UDI)

by Gimmi GmbH

Identity

Trade Name
Gimmi FDA UDI
Generic Name
Orthopaedic osteotome FDA UDI
Device Name
LAMBOTTE OSTEOTOME CURVED, 10 MM LENGTH 230 MM FDA UDI
Model / Reference
KM.1142.10 FDA UDI
Description
LAMBOTTE OSTEOTOME CURVED, 10 MM LENGTH 230 MM FDA UDI

Identifiers

Catalog Number
KM.1142.10 FDA UDI
Primary DI / UDI-DI
04049047708056 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic osteotome 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

Yes

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

Category: Orthopaedic osteotome

Gimmi, a cutting-edge orthopedic manual surgical instrument, is designed to provide precise and accurate bone cuts during orthopaedic procedures. With its curved, 10mm length and bevelled distal end, this single-use device offers improved control and flexibility in surgical settings.

Similar devices

Also classified as Orthopaedic osteotome.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gimmi GmbH

Sources (1)

  • FDA UDI eda6b167-9c59-4667-949c-210b56ba82da 35 fields · synced Jul 2, 2026