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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Biopsy drill bit FDA UDI
Device Name
COUNTERSINK, CANNULATED, 6.5 HEADLESS FDA UDI
Model / Reference
MSN20008 FDA UDI
Description
COUNTERSINK, CANNULATED, 6.5 HEADLESS FDA UDI

Identifiers

Catalog Number
MSN20008 FDA UDI
Primary DI / UDI-DI
10884389957219 FDA UDI
FDA Product Code
LXH FDA UDI
HWC FDA UDI
GMDN Term
Biopsy drill bit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
888.3040 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

Yes

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
MRI Safety
MR Unsafe FDA UDI

Category: Surgical countersink, reusableBiopsy drill bit

Medline by Medline Industries, 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

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI 95ff4764-f0d2-4877-888f-05b3d5b940eb 35 fields · synced May 30, 2026