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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
Hand-held surgical retractor, reusable FDA UDI
Device Name
Sims Vaginal Retr, 75x36mm, 9 3/4" FDA UDI
Model / Reference
46-0281 FDA UDI
Description
Sims Vaginal Retr, 75x36mm, 9 3/4" FDA UDI

Identifiers

Catalog Number
46-0281 FDA UDI
Primary DI / UDI-DI
00888515049185 FDA UDI
FDA Product Code
HDL FDA UDI
GMDN Term
Hand-held surgical retractor, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.4520 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: Hand-held surgical retractor, reusable

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

Similar devices

Also classified as Hand-held surgical retractor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d8109e5d-e075-4606-8452-49feffbdb55c 35 fields · synced Jun 9, 2026