Identity
- Trade Name
- PreVent Endo Holder FDA UDI
- Generic Name
- Endotracheal tube holder FDA UDI
- Device Name
- Endo Trach Tube Holder FDA UDI
- Model / Reference
- 790 FDA UDI
- Description
- Endo Trach Tube Holder FDA UDI
Identifiers
- Catalog Number
- 790 FDA UDI
- Primary DI / UDI-DI
- 10850014574625 FDA UDI
- FDA Product Code
- JAY FDA UDI
- GMDN Term
- Endotracheal tube holder FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5280 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
No
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
MR Safe FDA UDI
Category: Endotracheal tube holder
PreVent Endo Holder by Pepper Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Endotracheal tube holder.
- SunMed — SunMed · Class I
- Marpac Inc — Marpac, Inc. · Class I
- Curaplex — BOUND TREE MEDICAL, LLC · Class II
- PALA-NATE — Utah Medical Products, Inc. · Class II
- LINER FOAM TUBE SYSTEM — BIRD & CRONIN, LLC · Class I
- TRACH TUBE HOLDER ADULT, BULK — BIRD & CRONIN, LLC · Class I
- Curaplex — BOUND TREE MEDICAL, LLC · Class II
- SolidAIRity Flex — SECURISYN MEDICAL, LLC · Class I
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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Pepper Medical, Inc.
Sources (1)
- FDA UDI 8021d91c-1725-4d65-a565-81a17166e7d3 34 fields · synced Jun 8, 2026