Identity
- Trade Name
- BITE WING LOOPS FDA UDI
- Generic Name
- Dental x-ray film holder, single-use FDA UDI
- Model / Reference
- 6070553343 FDA UDI
Identifiers
- Primary DI / UDI-DI
- D89260705533431 FDA UDI
- FDA Product Code
- NRD FDA UDI
- GMDN Term
- Dental x-ray film holder, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.6640 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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 x-ray film holder, single-use
Bite Wing Loops by Maxill, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Dental x-ray film holder, single-use.
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- Steri-Shield — Steri-Shield Products, Inc. · Class I
- Steri-Shield — Steri-Shield Products, Inc. · Class I
- Universal Holders — SIRONA DENTAL, INC. · Class I
- Universal Holders — SIRONA DENTAL, INC. · Class I
- Intraoral Sensor Holder — SIRONA DENTAL, INC. · Class I
- Steri-Shield — Steri-Shield Products, Inc. · Class I
- Steri-Shield — Steri-Shield Products, 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 |
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Manufacturer
- Manufacturer
- Maxill, Inc.
Sources (1)
- FDA UDI e6960e33-bfa5-4ce6-a2f6-295d0f6d2be6 32 fields · synced Jun 8, 2026