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Loading Lindemann Guide Drill

FDA UDI

Class I (US FDA UDI)

by Ebi, LLC

Identity

Trade Name
Loading Lindemann Guide Drill FDA UDI
Generic Name
Dental implant system FDA UDI
Model / Reference
LLDL FDA UDI

Identifiers

Primary DI / UDI-DI
08809476189026 FDA UDI
FDA Product Code
EJL FDA UDI
GMDN Term
Dental implant system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3240 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant system

Loading Lindemann Guide Drill by Ebi, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ebi, LLC

Sources (1)

  • FDA UDI 13137aff-10d5-441b-86e9-faea2affcc6d 32 fields · synced May 30, 2026