Identity
- Trade Name
- Barcode wand FDA UDI
- Generic Name
- Barcode reader FDA UDI
- Device Name
- Barcode wand FDA UDI
- Model / Reference
- 0005312 FDA UDI
- Description
- Barcode wand FDA UDI
Identifiers
- Catalog Number
- 0005312 FDA UDI
- Primary DI / UDI-DI
- 08426950716419 FDA UDI
- FDA Product Code
- CHL FDA UDI
- GMDN Term
- Barcode reader FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1120 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
Yes
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Barcode reader
Barcode wand by Instrumentation Laboratory Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Barcode reader.
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- Tissue-Tek Film® — Sakura Finetek USA, Inc · Class I
- Bar Code Reader — ORPHEUS MEDICAL LTD · Class II
- Barcode Reader — Shenzhen Wisonic Medical Technology Co., Ltd. · Class II
- Tissue-Tek® Glas™ g2 — Sakura Finetek USA, 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 II | Pending data |
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Manufacturer
- Manufacturer
- Instrumentation Laboratory Company
Sources (1)
- FDA UDI e700ca70-51d2-4625-b0bf-162668739dc4 35 fields · synced Jun 8, 2026