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Integra® Miltex®

FDA UDI

Class I (US FDA UDI)

by Integra LifeSciences Production Corporation

Identity

Trade Name
Integra® Miltex® FDA UDI
Generic Name
Nasal file/rasp FDA UDI
Device Name
Integra® Miltex® Maltz Nasal Rasp 7", Straight, Forward Cutting FDA UDI
Model / Reference
PM-1452 FDA UDI
Description
Integra® Miltex® Maltz Nasal Rasp 7", Straight, Forward Cutting FDA UDI

Identifiers

Catalog Number
PM-1452 FDA UDI
Primary DI / UDI-DI
10381780451853 FDA UDI
FDA Product Code
HTR FDA UDI
GMDN Term
Nasal file/rasp FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 7 Inch FDA UDI

Category: Nasal file/rasp

A comprehensive and accurate description of the Integra Miltex nasal rasp, a medical device used in plastic surgery to remove and profile cartilage/bone. The device is made of metal, available in various sizes and working end designs, and can be sterilized using moist heat or steam.

Similar devices

Also classified as Nasal file/rasp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fbbb333c-9bb5-48e3-9128-202029b8ab70 36 fields · synced Jul 17, 2026