BOSS Instruments

FDA UDI

Class I (US FDA UDI)

by Boss Instruments, Ltd.

Identity

Trade Name: BOSS Instruments FDA UDI
Generic Name: Hand-held endoscopic retractor, reusable FDA UDI
Device Name: Five Finger Fan Retractor, Rigid, 95mm Sprd, 10mm shaft diameter, Flushable FDA UDI
Model / Reference: 35-7155 FDA UDI
Description: Five Finger Fan Retractor, Rigid, 95mm Sprd, 10mm shaft diameter, Flushable FDA UDI

Identifiers

Catalog Number: 35-7155 FDA UDI
Primary DI / UDI-DI: 00888515132856 FDA UDI
FDA Product Code: GAD FDA UDI
GMDN Term: Hand-held endoscopic retractor, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Hand-held endoscopic retractor, reusable

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

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Also classified as Hand-held endoscopic retractor, reusable.

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Snowden-Pencer — STERIS CORPORATION · Class II
Symmetry Lowsley — SYMMETRY SURGICAL INC. · Class I
Strauss Surgical — AMERICAN MEDICAL ENDOSCOPY · Class II
Snowden-Pencer — STERIS CORPORATION · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Boss Instruments, Ltd.

Sources (1)

FDA UDI 842b7ba6-0867-433b-83c3-1f18e5743af1 35 fields · synced Jun 9, 2026