Identity
- Trade Name
- Porta-View™ FDA UDI
- Generic Name
- Radiographic film view box, non-powered FDA UDI
- Device Name
- Post/Yoke for Porta-View™ FDA UDI
- Model / Reference
- 1018-A FDA UDI
- Description
- Post/Yoke for Porta-View™ FDA UDI
Identifiers
- Catalog Number
- 1018-A FDA UDI
- Primary DI / UDI-DI
- 00696588005836 FDA UDI
- FDA Product Code
- IXC FDA UDI
- GMDN Term
- Radiographic film view box, non-powered FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 892.1890 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Radiographic film view box, non-powered
Porta-View™ by Innovative Medical Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Radiographic film view box, non-powered.
- Porta-View™ — INNOVATIVE MEDICAL PRODUCTS, INC. · Class I
- Porta-View™ — INNOVATIVE MEDICAL PRODUCTS, INC. · Class I
- Porta-View™ — INNOVATIVE MEDICAL PRODUCTS, INC. · 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
- Innovative Medical Products, Inc.
Sources (1)
- FDA UDI 2af1ce0f-2df9-47a7-ae2a-929c541289bd 34 fields · synced May 30, 2026