Identity
- Trade Name
- Tuohy Epidural Needle FDA UDI
- Generic Name
- Epidural needle, non-threaded FDA UDI
- Device Name
- 17 ga (1.4 mm) x 9 cm FDA UDI
- Model / Reference
- TNMR-1703NS FDA UDI
- Description
- 17 ga (1.4 mm) x 9 cm FDA UDI
Identifiers
- Catalog Number
- TNMR-1703NS FDA UDI
- Primary DI / UDI-DI
- 00813079021605 FDA UDI
- FDA Product Code
- BSP FDA UDI
- GMDN Term
- Epidural needle, non-threaded FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5150 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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Needle Gauge — 17 Gauge FDA UDI
Category: Epidural needle, non-threaded
Tuohy Epidural Needle by Remington Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 a0ad56e7-21dd-463b-8b9f-cdec9b42970a 36 fields · synced Jun 8, 2026