Identity
- Trade Name
- MAX-JECT DENTAL NEEDLES FDA UDI
- Generic Name
- Dental anaesthesia syringe/needle FDA UDI
- Model / Reference
- 6070541355 FDA UDI
Identifiers
- Primary DI / UDI-DI
- D89260705413551 FDA UDI
- FDA Product Code
- DZM FDA UDI
- GMDN Term
- Dental anaesthesia syringe/needle 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
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
Category: Dental anaesthesia syringe/needle
Max-Ject Dental Needles by Maxill, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental anaesthesia syringe/needle.
- Pre-Bent Flow Tips — Dynarex Corp. · Class I
- Pre-Bent Flow Tips — Dynarex Corp. · Class I
- Pre-Bent Flow Tips — Dynarex Corp. · Class I
- Pre-Bent Flow Tips — Dynarex Corp. · Class I
- MAX-JECT DENTAL NEEDLES — MAXILL, INC. · Class I
- MAX-JECT DENTAL NEEDLES — MAXILL, INC. · Class I
- MAX-JECT DENTAL NEEDLES — MAXILL, INC. · Class I
- MAX-JECT DENTAL NEEDLES — MAXILL, INC. · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Maxill, Inc.
Sources (1)
- FDA UDI 5b1465d0-5b0e-420a-93ea-39240fe00247 32 fields · synced Jun 8, 2026