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Simple Guide Plus Sleeve Connector

FDA UDIEUDAMED

Class I (US FDA UDI)

by Dentis Co. , Ltd

Identity

Trade Name
Simple Guide Plus Sleeve Connector FDA UDI
Generic Name
Dental appliance/prosthesis connector FDA UDI
Device Name
Dental Implant Instrument / Simple Guide Plus Sleeve Connector FDA UDI
Model / Reference
DSGPSC FDA UDI
Description
Dental Implant Instrument / Simple Guide Plus Sleeve Connector FDA UDI

Identifiers

Primary DI / UDI-DI
08800053004701 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental appliance/prosthesis connector FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental appliance/prosthesis connector

Simple Guide Plus Sleeve Connector by Dentis Co. , Ltd — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance/prosthesis connector.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dentis Co. , Ltd

Sources (2)

  • FDA UDI 55577552-036a-4661-9745-b17997b757cc 33 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 18, 2026