Identity
- Trade Name
- EXMOOR FDA UDI
- Generic Name
- Secretion suction kit FDA UDI
- Device Name
- Myringotomy Kit with Grommets FDA UDI
- Model / Reference
- MK/82/A/N/E102 FDA UDI
- Description
- Myringotomy Kit with Grommets FDA UDI
Identifiers
- Catalog Number
- MK82ANE102 FDA UDI
- Primary DI / UDI-DI
- 05060180252632 FDA UDI
- FDA Product Code
- JYP FDA UDI
- GMDN Term
- Secretion suction kit FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4420 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
Yes
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: Secretion suction kit
Exmoor by Exmoor Plastics , Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Bioseal Inc. — BIOSEAL · Class I
- Suction Kit — SUNSET HEALTHCARE SOLUTIONS, Inc.
- Suction Component Kit — SUNSET HEALTHCARE SOLUTIONS, Inc.
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
- Exmoor Plastics , Ltd.
Sources (1)
- FDA UDI db0d844e-ae82-42fe-bb6d-3ff2b80dba1a 36 fields · synced Jun 8, 2026