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Figure 8 Sternotomy Closure Device

FDA UDI

Class II (US FDA UDI)

by Figure 8 Surgical, Inc.

Identity

Trade Name
Figure 8 Sternotomy Closure Device FDA UDI
Generic Name
Sternal fixation device FDA UDI
Device Name
Shelf Box for Single Straps FDA UDI
Model / Reference
FP-20188 FDA UDI
Description
Shelf Box for Single Straps FDA UDI

Identifiers

Primary DI / UDI-DI
10862376000322 FDA UDI
FDA Product Code
JDQ FDA UDI
GMDN Term
Sternal fixation device FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3010 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Category: Sternal fixation device

Figure 8 Sternotomy Closure Device by Figure 8 Surgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sternal fixation device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 61bdbc9c-4a34-48b2-b719-86e142193735 34 fields · synced Jun 6, 2026