Identity
- Trade Name
- Closed Needle Guide FDA UDI
- Generic Name
- Needle guide, single-use FDA UDI
- Device Name
- 14ga (2.1mm) FDA UDI
- Model / Reference
- LNGC-14 FDA UDI
- Description
- 14ga (2.1mm) FDA UDI
Identifiers
- Catalog Number
- LNGC-14 FDA UDI
- Primary DI / UDI-DI
- 00813079020400 FDA UDI
- 510(k) Number
- K983621 FDA UDI
- FDA Product Code
- IZH FDA UDI
- GMDN Term
- Needle guide, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1710 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Ethylene Oxide FDA UDI
Dimensions & Sizes
- Size
- Needle Gauge — 14 Gauge FDA UDI
Category: Needle guide, single-use
Closed Needle Guide by Remington Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Needle guide, single-use.
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Cleared under the same submission
K983621 also covers:
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
- Remington Medical, Inc.
Sources (1)
- FDA UDI 999f8b8a-94f4-418c-a57f-54edfc4278b7 37 fields · synced Jun 8, 2026