Identity
- Trade Name
- Plasdent FDA UDI
- Generic Name
- X-ray film cassette holder FDA UDI
- Device Name
- Notched Film Mount - 1W, 1H#2 FDA UDI
- Model / Reference
- NH-1H2 FDA UDI
- Description
- Notched Film Mount - 1W, 1H#2 FDA UDI
Identifiers
- Catalog Number
- NH-1H2 FDA UDI
- Primary DI / UDI-DI
- D832NH1H21 FDA UDI
- FDA Product Code
- NRD FDA UDI
- GMDN Term
- X-ray film cassette holder FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.6640 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: X-ray film cassette holder
Plasdent by Plasdent Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as X-ray film cassette holder.
- QT-LCH — CARESTREAM HEALTH, INC. · Class I
- SEDECAL — Sedecal., Sa. · Class I
- Mindray — Nanjing Mindray Bio-Medical Electronics Co., Ltd · Class I
- dose-map™ — Ashland Specialty Ingredients, G.P. · Class II
- Q-DRT-DRXT-R — CARESTREAM HEALTH, INC. · Class II
- OPERON — STRYKER Communications, Inc. · Class I
- LLD 129 Compact — Drtech Corp. · Class I
- dose-map™ — Ashland Specialty Ingredients, G.P. · Class II
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
- Plasdent Corp.
Sources (1)
- FDA UDI 70a52cfd-1290-49bb-b97b-b37ec61491c6 34 fields · synced May 31, 2026