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Zavation

FDA UDI

Class I (US FDA UDI)

by Zavation

Identity

Trade Name
Zavation FDA UDI
Generic Name
Bone tap, reusable FDA UDI
Device Name
Custom Tap/8.5mm FDA UDI
Model / Reference
ZAV-1334-85 FDA UDI
Description
Custom Tap/8.5mm FDA UDI

Identifiers

Primary DI / UDI-DI
00197157006211 FDA UDI
510(k) Number
K112533 FDA UDI
FDA Product Code
LXH FDA UDI
KWQ FDA UDI
GMDN Term
Bone tap, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
888.3060 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

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone tap, reusable

Zavation by Zavation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone tap, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zavation

Sources (1)

  • FDA UDI d4cf8f2b-98fb-49b1-bfca-ccbc660a40e0 35 fields · synced May 30, 2026