← Back to catalogue

Integra® Miltex®

FDA UDI

Class I (US FDA UDI)

by Integra LifeSciences Production Corporation

Identity

Trade Name
Integra® Miltex® FDA UDI
Generic Name
Dental laboratory mandrel FDA UDI
Device Name
Integra® Miltex® Mandrel, Loma Linda, Thin Head, Right Angle - 12 Pack FDA UDI
Model / Reference
DM350RA FDA UDI
Description
Integra® Miltex® Mandrel, Loma Linda, Thin Head, Right Angle - 12 Pack FDA UDI

Identifiers

Catalog Number
DM350RA FDA UDI
Primary DI / UDI-DI
10381780507260 FDA UDI
FDA Product Code
EHJ FDA UDI
GMDN Term
Dental laboratory mandrel FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6010 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

No

FDA UDI

Category: Dental laboratory mandrel

Integra® Miltex® by Integra LifeSciences Production Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental laboratory mandrel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 5576dc7c-30d0-42d3-8421-3cbdee9d56b7 35 fields · synced Jun 9, 2026