← Back to catalogue

Bone Marrow "J" Needle Double Diamond Tip

FDA UDI

Class I (US FDA UDI)

by Remington Medical, Inc.

Identity

Trade Name
Bone Marrow "J" Needle Double Diamond Tip FDA UDI
Generic Name
Bone marrow biopsy needle, single-use FDA UDI
Device Name
11ga (3.0mm) x 6in. (15cm) FDA UDI
Model / Reference
JD-1106 FDA UDI
Description
11ga (3.0mm) x 6in. (15cm) FDA UDI

Identifiers

Catalog Number
JD-1106 FDA UDI
Primary DI / UDI-DI
00813079020257 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
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Needle Gauge — 11 Gauge FDA UDI

Category: Bone marrow biopsy needle, single-use

Bone Marrow "J" Needle Double Diamond Tip by Remington Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone marrow biopsy needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 0d2626c4-b20a-4b8b-89cc-04b841110a10 36 fields · synced Jun 8, 2026