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Cannulated Drill 3.03.5mm

FDA UDI

Class I (US FDA UDI)

by Biopro, Inc.

Identity

Trade Name
CANNULATED DRILL 3.03.5MM FDA UDI
Generic Name
Cannulated surgical drill bit, single-use FDA UDI
Model / Reference
18333 FDA UDI

Identifiers

Primary DI / UDI-DI
00810012485272 FDA UDI
510(k) Number
K083490 FDA UDI
FDA Product Code
HTW FDA UDI
GMDN Term
Cannulated 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cannulated surgical drill bit, single-use

Cannulated Drill 3.03.5mm by Biopro, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biopro, Inc.

Sources (1)

  • FDA UDI 303d1193-3dc5-4fbb-9161-e16fe2e86ea9 33 fields · synced May 30, 2026