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BOSS Instruments

FDA UDI

Class I (US FDA UDI)

by Boss Instruments, Ltd.

Identity

Trade Name
BOSS Instruments FDA UDI
Generic Name
Surgical drill chuck FDA UDI
Device Name
Drill Bit Jacob Chuck end 4.7mm, 127mm OAL, flute length 53mm FDA UDI
Model / Reference
79-0478 FDA UDI
Description
Drill Bit Jacob Chuck end 4.7mm, 127mm OAL, flute length 53mm FDA UDI

Identifiers

Catalog Number
79-0478 FDA UDI
Primary DI / UDI-DI
00888515204881 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Surgical drill chuck 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical drill chuck

BOSS Instruments by Boss Instruments, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical drill chuck.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e717b127-dc85-4fe0-af36-5e35897ea7b1 35 fields · synced Jun 9, 2026