Identity
- Trade Name
- JEDMED FDA UDI
- Generic Name
- Dental implant suprastructure reamer guide FDA UDI
- Device Name
- Suction System Package FDA UDI
- Model / Reference
- 03-5544 FDA UDI
- Description
- Suction System Package FDA UDI
Identifiers
- Catalog Number
- 03-5544 FDA UDI
- Primary DI / UDI-DI
- M6330355440 FDA UDI
- FDA Product Code
- GCX FDA UDI
- GMDN Term
- Dental implant suprastructure reamer guide FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 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
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
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: Dental implant suprastructure reamer guide
Jedmed by JEDMED Instrument Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental implant suprastructure reamer guide.
- Preat — PREAT Corporation · Class I
- DENTECH — Dentech Corp. · Class I
- Preat — PREAT Corporation · Class I
- Gauge for reamer — Thommen Medical AG · Class I
- Preat — PREAT Corporation · 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 II | Pending data |
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Manufacturer
- Manufacturer
- JEDMED Instrument Company
Sources (1)
- FDA UDI 0dd178c3-c359-4939-8447-ecf55fd9121b 35 fields · synced Jun 6, 2026