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
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Cleared under the same submission
K830090 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Teleflex Incorporated
Sources (1)
- FDA UDI 5fb5cdba-b2a3-4d40-a4ab-fff43c119611 36 fields · synced May 30, 2026