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Calibrated Drill 5.0mm X 365mm

FDA UDI

Class I (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name
CALIBRATED DRILL 5.0MM X 365MM FDA UDI
Generic Name
Biopsy drill bit FDA UDI
Model / Reference
27982 FDA UDI

Identifiers

Catalog Number
27982 FDA UDI
Primary DI / UDI-DI
00880304500464 FDA UDI
FDA Product Code
HTW FDA UDI
GMDN Term
Biopsy drill bit 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

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Category: Biopsy drill bit

Calibrated Drill 5.0mm X 365mm by Biomet Orthopedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Biopsy drill bit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2e2fa725-de1b-4816-aaf9-37d83a920253 34 fields · synced Jun 8, 2026