Geminus

FDA UDI

Class II (US FDA UDI)

by Skeletal Dynamics L.l.c.

Identity

Trade Name: Geminus FDA UDI
Generic Name: Fluted surgical drill bit, single-use FDA UDI
Model / Reference: Drill, Solid Side Cutting, 2.0mm x 40mm FDA UDI

Identifiers

Catalog Number: DRLL-SSC-20040 FDA UDI
Primary DI / UDI-DI: 00841506101255 FDA UDI
FDA Product Code: HRS FDA UDI
GMDN Term: Fluted surgical drill bit, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3030 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 2 Millimeter FDA UDI

Category: Fluted surgical drill bit, single-use

Geminus by Skeletal Dynamics L.l.c. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Skeletal Dynamics L.l.c.

Sources (1)

FDA UDI dc9e0167-c19e-4b97-8932-3e544e11fd5e 35 fields · synced May 30, 2026