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FeatherTouch®

FDA UDI

Class II (US FDA UDI)

by Medtronic Xomed, Inc.

Identity

Trade Name
FeatherTouch® FDA UDI
Generic Name
Nasal file/rasp FDA UDI
Device Name
RASP 1992208 FEATHERTOUCH 2PK COARSE FDA UDI
Model / Reference
1992208 FDA UDI
Description
RASP 1992208 FEATHERTOUCH 2PK COARSE FDA UDI

Identifiers

Primary DI / UDI-DI
20681490051525 FDA UDI
510(k) Number
K983025 FDA UDI
FDA Product Code
HRX FDA UDI
GMDN Term
Nasal file/rasp FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Width — 8.0 Millimeter FDA UDI

Category: Nasal file/rasp

FeatherTouch® by Medtronic Xomed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal file/rasp.

Cleared under the same submission

K983025 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 20c77688-770f-472e-8ee7-940f24c94793 36 fields · synced Jun 1, 2026