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Hudson Rci

FDA UDI

Class II (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
HUDSON RCI FDA UDI
Generic Name
Seizure bite block FDA UDI
Device Name
Disposable Bite Stick Bite Block/Tongue Depressor FDA UDI
Model / Reference
IPN041777 FDA UDI
Description
Disposable Bite Stick Bite Block/Tongue Depressor FDA UDI

Identifiers

Catalog Number
1174 FDA UDI
Primary DI / UDI-DI
14026704580221 FDA UDI
510(k) Number
K830090 FDA UDI
FDA Product Code
JXL FDA UDI
GMDN Term
Seizure bite block FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5070 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Seizure bite block

Hudson Rci by Teleflex Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Seizure bite block.

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 5fb5cdba-b2a3-4d40-a4ab-fff43c119611 36 fields · synced May 30, 2026