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Stealth Surgical

FDA UDI

Class II (US FDA UDI)

by Boss Instruments, Ltd.

Identity

Trade Name
Stealth Surgical FDA UDI
Generic Name
Laminectomy retractor, self-retaining FDA UDI
Device Name
STEALTH CPS BASE TRAY FDA UDI
Model / Reference
SS1671719 FDA UDI
Description
STEALTH CPS BASE TRAY FDA UDI

Identifiers

Catalog Number
SS1671719 FDA UDI
Primary DI / UDI-DI
00888515261662 FDA UDI
FDA Product Code
GZT FDA UDI
GMDN Term
Laminectomy retractor, self-retaining FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4800 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: Laminectomy retractor, self-retaining

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

Similar devices

Also classified as Laminectomy retractor, self-retaining.

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 96eddd2e-a31b-4736-938c-a6e24d6d8674 35 fields · synced Jun 9, 2026