Identity
- Trade Name
- ORABLOC FDA UDI
- Generic Name
- Dental syringe needle, single-use FDA UDI
- Device Name
- Orabloc Needle twenty5L FDA UDI
- Model / Reference
- Orabloc Needle twenty5L FDA UDI
- Description
- Orabloc Needle twenty5L FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08053610771886 FDA UDI
- FDA Product Code
- DZM FDA UDI
- GMDN Term
- Dental syringe needle, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4730 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
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Needle Gauge — 25 Gauge FDA UDI
Category: Dental syringe needle, single-use
Orabloc by Tecnofar Spa — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Dental syringe needle, single-use.
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- V-Ject — VERICOM CO., LTD. · Class I
- Darby Dental Supply, LLC — DARBY DENTAL SUPPLY, LLC · Class I
- V-Ject — VERICOM CO., LTD. · Class I
- SEPTOJECT 30G SHORT — SEPTODONT SAS SPECIALITES SEPTODONT · 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
- Tecnofar Spa
Sources (1)
- FDA UDI fa3cd541-ee23-43d1-9c9b-3d2471341b56 35 fields · synced May 30, 2026