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Global Apg+

FDA UDI

Class I (US FDA UDI)

by Depuy (ireland)

Identity

Trade Name
GLOBAL APG+ FDA UDI
Generic Name
Fluted surgical drill bit, single-use FDA UDI
Device Name
GLOBAL APG+ QUICK CONNECT CENTRAL DRILL BIT 48,52,56 FDA UDI
Model / Reference
2236-00-015 FDA UDI
Description
GLOBAL APG+ QUICK CONNECT CENTRAL DRILL BIT 48,52,56 FDA UDI

Identifiers

Catalog Number
223600015 FDA UDI
Primary DI / UDI-DI
10603295105824 FDA UDI
FDA Product Code
HTW FDA UDI
GMDN Term
Fluted surgical drill bit, single-use 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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: Fluted surgical drill bit, single-use

Global Apg+ by Depuy (ireland) — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluted surgical drill bit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Depuy (ireland)

Sources (1)

  • FDA UDI a1fa306b-049f-4ef0-afe8-e4a6205c4d54 35 fields · synced May 31, 2026