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Bone Awl

FDA UDI

Class I (US FDA UDI)

by RZ-Medizintechnik GmbH

Identity

Trade Name
Bone Awl FDA UDI
Generic Name
General surgery wound probe/packer FDA UDI
Device Name
Bone Awl, 3.0 x 330mm FDA UDI
Model / Reference
259-430-310 FDA UDI
Description
Bone Awl, 3.0 x 330mm FDA UDI

Identifiers

Primary DI / UDI-DI
04049197515061 FDA UDI
FDA Product Code
FZO FDA UDI
GMDN Term
General surgery wound probe/packer 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

No

FDA UDI

Single Use

No

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: General surgery wound probe/packer

Bone Awl by RZ-Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General surgery wound probe/packer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
RZ-Medizintechnik GmbH

Sources (1)

  • FDA UDI 17965566-4897-4103-a172-331689d0ef22 33 fields · synced Jun 6, 2026