Identity
- Trade Name
- EXMOOR FDA UDI
- Generic Name
- Otological bone particle collector FDA UDI
- Device Name
- Bone Pate Collector Filters Pack FDA UDI
- Model / Reference
- E402 FDA UDI
- Description
- Bone Pate Collector Filters Pack FDA UDI
Identifiers
- Catalog Number
- E402 FDA UDI
- Primary DI / UDI-DI
- 05060180256180 FDA UDI
- FDA Product Code
- MXP FDA UDI
- GMDN Term
- Otological bone particle collector FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Otological bone particle collector
Exmoor by Exmoor Plastics , Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Otological bone particle collector.
- SHEEHY BONE DUST COLLECTOR — Oto-Med, Inc. · Class I
- COX BONE DUST COLLECTOR — Oto-Med, Inc. · Class I
- EXMOOR — Exmoor Plastics , Ltd. · 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
- Exmoor Plastics , Ltd.
Sources (1)
- FDA UDI eec11a29-22f2-4fdf-8183-5c41293ed0de 36 fields · synced Jun 8, 2026