Identity
- Trade Name
- MectaPlug FDA UDI
- Generic Name
- Polymer orthopaedic cement restrictor, bioabsorbable FDA UDI
- Model / Reference
- Diameter 14 FDA UDI
Identifiers
- Catalog Number
- 01.33.004 FDA UDI
- Primary DI / UDI-DI
- 03760177044029 FDA UDI
- FDA Product Code
- LZN FDA UDI
- GMDN Term
- Polymer orthopaedic cement restrictor, bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.3300 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 14 Millimeter FDA UDI
Category: Polymer orthopaedic cement restrictor, bioabsorbable
MectaPlug by Teknimed — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Polymer orthopaedic cement restrictor, bioabsorbable.
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 II | Pending data |
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Manufacturer
- Manufacturer
- Teknimed
Sources (1)
- FDA UDI 6982fb29-8cb5-4dce-a137-6f6dde7cdf80 34 fields · synced Jun 1, 2026