Identity
- Trade Name
- Bone Marrow "I" Needle FDA UDI
- Generic Name
- Bone marrow biopsy needle, single-use FDA UDI
- Device Name
- 15ga (1.8mm) x 1 7/8" (5cm) FDA UDI
- Model / Reference
- 1501-I FDA UDI
- Description
- 15ga (1.8mm) x 1 7/8" (5cm) FDA UDI
Identifiers
- Catalog Number
- 1501-I FDA UDI
- Primary DI / UDI-DI
- 00813079020226 FDA UDI
- FDA Product Code
- GAA FDA UDI
- GMDN Term
- Bone marrow biopsy 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 — 15 Gauge FDA UDI
Category: Bone marrow biopsy needle, single-use
Bone Marrow "I" Needle by Remington Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Bone marrow biopsy needle, single-use.
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- Monoject — Cardinalhealth · Class II
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- Faset — Dio Medical Co., Ltd. · U
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 6e8c3fe1-c989-4c91-a987-e6cc8ed1d0ce 36 fields · synced Jun 8, 2026