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Boss Instruments

FDA UDI

Class II (US FDA UDI)

by Boss Instruments, Ltd.

Identity

Trade Name
Boss Instruments FDA UDI
Generic Name
Spinal rongeur FDA UDI
Device Name
APEX Rongeur, Tarpon, 8" (200mm) 4mm, 40° up, Stainless Steel Updated Tip Design FDA UDI
Model / Reference
70-2915N FDA UDI
Description
APEX Rongeur, Tarpon, 8" (200mm) 4mm, 40° up, Stainless Steel Updated Tip Design FDA UDI

Identifiers

Catalog Number
70-2915N FDA UDI
Primary DI / UDI-DI
00888515299405 FDA UDI
FDA Product Code
HAE FDA UDI
GMDN Term
Spinal rongeur FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4840 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Spinal rongeur

Boss Instruments by Boss Instruments, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal rongeur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boss Instruments, Ltd.

Sources (1)

  • FDA UDI 043ce9da-e8a6-470d-8cff-4e46dc598205 35 fields · synced Jun 9, 2026