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Bp®

FDA UDI

Class II (US FDA UDI)

by Zimmer Spine, Inc.

Identity

Trade Name
BP® FDA UDI
Generic Name
Intervertebral-body internal spinal fixation system FDA UDI
Model / Reference
8002-1720-00 FDA UDI

Identifiers

Catalog Number
8002-1720-00 FDA UDI
Primary DI / UDI-DI
00889024338562 FDA UDI
FDA Product Code
MAX FDA UDI
GMDN Term
Intervertebral-body internal spinal fixation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 20 Millimeter FDA UDI
Outer Diameter — 17 Millimeter FDA UDI

Category: Intervertebral-body internal spinal fixation system

Bp® by Zimmer Spine, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intervertebral-body internal spinal fixation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer Spine, Inc.

Sources (1)

  • FDA UDI 5478ccbb-9b61-4de8-877e-c698ab562763 35 fields · synced Jun 8, 2026