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E300 Post Delivery System

FDA UDI

Class I (US FDA UDI)

by Engle Dental Systems

Identity

Trade Name
E300 Post Delivery System FDA UDI
Generic Name
Dental delivery system instrument unit, pneumatic FDA UDI
Device Name
E300 Dr's post mount delivery system FDA UDI
Model / Reference
P070935 FDA UDI
Description
E300 Dr's post mount delivery system FDA UDI

Identifiers

Catalog Number
P070935 FDA UDI
Primary DI / UDI-DI
00850043433330 FDA UDI
510(k) Number
K983285 FDA UDI
FDA Product Code
EIA FDA UDI
GMDN Term
Dental delivery system instrument unit, pneumatic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6640 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental delivery system instrument unit, pneumatic

E300 Post Delivery System by Engle Dental Systems — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental delivery system instrument unit, pneumatic.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c4970063-78d9-40b9-8472-dbec7d4a654e 36 fields · synced Jun 6, 2026