← Back to catalogue

Sheehy-House Powder Insufflator

FDA UDI

Class I (US FDA UDI)

by Oto-Med, Inc.

Identity

Trade Name
SHEEHY-HOUSE POWDER INSUFFLATOR FDA UDI
Generic Name
ENT powder applicator FDA UDI
Device Name
SHEEHY-HOUSE POWDER INSUFFLATOR FDA UDI
Model / Reference
S-3001 FDA UDI
Description
SHEEHY-HOUSE POWDER INSUFFLATOR FDA UDI

Identifiers

Primary DI / UDI-DI
00850000126053 FDA UDI
FDA Product Code
KCL FDA UDI
GMDN Term
ENT powder applicator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.5220 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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: ENT powder applicator

Sheehy-House Powder Insufflator by Oto-Med, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ENT powder applicator.

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

Manufacturer
Oto-Med, Inc.

Sources (1)

  • FDA UDI e4b05966-8629-4c1d-8d2a-d55014661fec 34 fields · synced Jun 8, 2026