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Bedford™

FDA UDI

Class I (US FDA UDI)

by Merit Medical Systems, Inc.

Identity

Trade Name
Bedford™ FDA UDI
Generic Name
Bone biopsy needle FDA UDI
Model / Reference
00884450411872 FDA UDI

Identifiers

Primary DI / UDI-DI
00884450411872 FDA UDI
FDA Product Code
GAA FDA UDI
GMDN Term
Bone biopsy needle 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Category: Bone biopsy needle

Bedford is a sterile, sharp bevel-edged, hollow tubular metal instrument designed to obtain specimens of bone, bone marrow, and/or tumors from any bone of the body. This single-use device is typically inserted through a bone access cannula under imaging control and supplied with an ejector rod to remove the biopsy.

Similar devices

Also classified as Bone biopsy needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Merit Medical Systems, Inc.

Sources (1)

  • FDA UDI c0cdbc07-9718-4077-8aff-82f5ce51b819 32 fields · synced Jul 18, 2026