← Back to catalogue

BOSS Instruments

FDA UDI

Class I (US FDA UDI)

by Boss Instruments, Ltd.

Identity

Trade Name
BOSS Instruments FDA UDI
Generic Name
Surgical soft-tissue manipulation forceps, alligator, reusable FDA UDI
Device Name
Kleinsasser Mini Fcp, cvd up, 1mm cup FDA UDI
Model / Reference
95-9151 FDA UDI
Description
Kleinsasser Mini Fcp, cvd up, 1mm cup FDA UDI

Identifiers

Catalog Number
95-9151 FDA UDI
Primary DI / UDI-DI
00888515249073 FDA UDI
FDA Product Code
KAE FDA UDI
GMDN Term
Surgical soft-tissue manipulation forceps, alligator, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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: Surgical soft-tissue manipulation forceps, alligator, reusable

BOSS Instruments' Surgical Soft-Tissue Manipulation Forceps are a reusable, alligator-style instrument designed for precise ear, nose, and throat (ENT) surgery. These instruments facilitate grasping and manipulation of soft tissues, typically during surgical procedures involving the ears, noses, and throats.

Similar devices

Also classified as Surgical soft-tissue manipulation forceps, alligator, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI a9226eed-9999-405e-b973-c8d2c4512a5f 35 fields · synced Jul 19, 2026