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Drill bit AO QC 3.2 x 145/120mm, Sterile

FDA UDI

Class I (US FDA UDI)

by Biopro, Inc.

Identity

Trade Name
Drill bit AO QC 3.2 x 145/120mm, Sterile FDA UDI
Generic Name
Surgical drill guide, single-use, non-sterile FDA UDI
Model / Reference
OL32DBS FDA UDI

Identifiers

Primary DI / UDI-DI
00810012483520 FDA UDI
FDA Product Code
HTW FDA UDI
GMDN Term
Surgical drill guide, single-use, non-sterile 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical drill guide, single-use, non-sterile

Drill bit AO QC 3.2 x 145/120mm, Sterile by Biopro, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical drill guide, single-use, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biopro, Inc.

Sources (1)

  • FDA UDI 6888673c-c1ea-480f-b75c-a421ab4ce089 32 fields · synced May 31, 2026