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BOSS Instruments

FDA UDI

Class I (US FDA UDI)

by Boss Instruments, Ltd.

Identity

Trade Name
BOSS Instruments FDA UDI
Generic Name
Suturing needle holder, reusable FDA UDI
Device Name
Rhoton Style NH, bayonet, cvd, .9mm tip, Ti, 9 1/2" FDA UDI
Model / Reference
72-8549T FDA UDI
Description
Rhoton Style NH, bayonet, cvd, .9mm tip, Ti, 9 1/2" FDA UDI

Identifiers

Catalog Number
72-8549T FDA UDI
Primary DI / UDI-DI
00888515176645 FDA UDI
FDA Product Code
GZX FDA UDI
GMDN Term
Suturing needle holder, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.4525 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

Yes

FDA UDI

Lot / Batch Number

Yes

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: Suturing needle holder, reusable

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

Similar devices

Also classified as Suturing needle holder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f75df9ee-5aa6-47d2-b8ee-839e8d297910 35 fields · synced Jun 9, 2026