Identity
- Trade Name
- Chiba Needle Marked FDA UDI
- Generic Name
- Body aspiration needle, single-use FDA UDI
- Device Name
- 22ga (0.7mm) x 18cm FDA UDI
- Model / Reference
- CNM-2207 FDA UDI
- Description
- 22ga (0.7mm) x 18cm FDA UDI
Identifiers
- Catalog Number
- CNM-2207 FDA UDI
- Primary DI / UDI-DI
- 00813079020622 FDA UDI
- FDA Product Code
- GAA FDA UDI
- GMDN Term
- Body aspiration needle, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
Ethylene Oxide FDA UDI
Dimensions & Sizes
- Size
- Needle Gauge — 22 Gauge FDA UDI
Category: Body aspiration needle, single-use
Chiba Needle Marked by Remington Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Body aspiration needle, single-use.
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- MReye — COOK INCORPORATED · Class II
- CHIBA SONO — Pajunk GmbH Medizintechnologie · Class II
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
- Remington Medical, Inc.
Sources (1)
- FDA UDI 9a2dca2f-9c8d-4454-a2f8-ac4a3d5b5525 36 fields · synced Jun 8, 2026