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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
SBX-28-R FDA UDI

Identifiers

Primary DI / UDI-DI
00850051972715 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

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

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 — 2.8 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

Similar devices

Also classified as Fluted surgical drill bit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Loocid Llc

Sources (1)

  • FDA UDI 973b656a-224f-4ff8-9be3-590ebc22e01c 35 fields · synced May 31, 2026