Identity
- Trade Name
- Surgical Direct FDA UDI
- Generic Name
- Dental rongeur FDA UDI
- Device Name
- American Extraction Forceps, 53L, Upper Molar FDA UDI
- Model / Reference
- SD48130 FDA UDI
- Description
- American Extraction Forceps, 53L, Upper Molar FDA UDI
Identifiers
- Catalog Number
- SD48130 FDA UDI
- Primary DI / UDI-DI
- B382SD481300 FDA UDI
- FDA Product Code
- EIX FDA UDI
- GMDN Term
- Dental rongeur FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4565 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
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
Moist Heat or Steam Sterilization FDA UDI
Category: Dental rongeur
Surgical Direct by Surgical Direct, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Dental rongeur.
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- STOMA® — Storz am Mark GmbH · Class I
- BMT Medizintechnik GmbH — BMT Medizintechnik GmbH · 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 |
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Manufacturer
- Manufacturer
- Surgical Direct, Inc.
Sources (1)
- FDA UDI 7f13f11a-0aea-4afe-8d69-257070177a68 35 fields · synced Jun 1, 2026