Loocid BCP

FDA UDI

Class I (US FDA UDI)

by Loocid Llc

Identity

Trade Name: Loocid BCP FDA UDI
Generic Name: Fluted surgical drill bit, reusable FDA UDI
Model / Reference: DB-UNI-30-20-R FDA UDI

Identifiers

Primary DI / UDI-DI: 00850055961111 FDA UDI
FDA Product Code: DZA FDA UDI
GMDN Term: Fluted surgical drill bit, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.4130 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

MRI Safety

MR Unsafe FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 2.0 Millimeter FDA UDI

Category: Fluted surgical drill bit, reusable

Loocid BCP by Loocid Llc — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Loocid Llc

Sources (1)

FDA UDI 03865f04-e948-47e8-8f04-340cc79aadd3 35 fields · synced May 31, 2026