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ZGO C-Guide Sleeve

FDA UDI

Class N (US FDA UDI)

by Versah, Llc

Identity

Trade Name
ZGO C-Guide Sleeve FDA UDI
Generic Name
Surgical instrument interim-placement holder, reusable FDA UDI
Device Name
ZGO C-Guide Sleeve is placed into ZGO surgical guide by the dental las as appropriate for each patient anatomy and treatment plan. FDA UDI
Model / Reference
ZCG FDA UDI
Description
ZGO C-Guide Sleeve is placed into ZGO surgical guide by the dental las as appropriate for each patient anatomy and treatment plan. FDA UDI

Identifiers

Primary DI / UDI-DI
00850017652750 FDA UDI
FDA Product Code
NAP FDA UDI
GMDN Term
Surgical instrument interim-placement holder, reusable FDA UDI

Classification

Device Class
N FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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 instrument interim-placement holder, reusable

ZGO C-Guide Sleeve by Versah, Llc — Class N — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument interim-placement holder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Versah, Llc

Sources (1)

  • FDA UDI 840df25b-0116-46ba-9d2b-640cd9a5f829 34 fields · synced May 30, 2026