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Drill Guide Adjustable

FDA UDI

Class I (US FDA UDI)

by Biopro, Inc.

Identity

Trade Name
DRILL GUIDE ADJUSTABLE FDA UDI
Generic Name
Surgical drill guide, single-use FDA UDI
Model / Reference
17681 FDA UDI

Identifiers

Primary DI / UDI-DI
00810012483865 FDA UDI
510(k) Number
K061798 FDA UDI
FDA Product Code
FZX FDA UDI
GMDN Term
Surgical drill guide, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: Surgical drill guide, single-use

Drill Guide Adjustable 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.

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 8e819c6d-6752-459f-84ec-91b444dfa8aa 33 fields · synced May 30, 2026