Identity
- Trade Name
- Aquaplast PS™ FDA UDI
- Generic Name
- External nasal splint FDA UDI
- Device Name
- Ivory, 3/32" Small, Dr. Silver's Stents Extended Length, Silver Style Stent FDA UDI
- Model / Reference
- PS-1736 FDA UDI
- Description
- Ivory, 3/32" Small, Dr. Silver's Stents Extended Length, Silver Style Stent FDA UDI
Identifiers
- Catalog Number
- PS-1736 FDA UDI
- Primary DI / UDI-DI
- 10841962107836 FDA UDI
- FDA Product Code
- EPP FDA UDI
- GMDN Term
- External nasal splint FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.5800 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
MR Safe FDA UDI
Dimensions & Sizes
- Size
- Depth — 0.094 Inch FDA UDI
Category: External nasal splint
Aquaplast PS™ by Qfix — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as External nasal splint.
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- DENVER SPLINT — Summit Medical, LLC · Class I
- BRIDGEMASTER™ — MEDTRONIC XOMED, INC. · Class I
- DENVER SPLINT — Summit Medical, LLC · Class I
- Equipment box for external nasal splints — Spiggle & Theis Medizintechnik GmbH · Class I
- DENVER SPLINT — Summit 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 |
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Manufacturer
- Manufacturer
- Qfix
Sources (1)
- FDA UDI 9d700258-c0b1-4129-96d3-b679cc454d3e 36 fields · synced May 31, 2026