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BR Surgical, LLC

FDA UDI

Class I (US FDA UDI)

by Br Surgical Llc

Identity

Trade Name
BR Surgical, LLC FDA UDI
Generic Name
Obstetrical/gynaecological surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
Disposable IUD Sterile Kit, (5) per box: tenaculum forcep, stitch scissor, swabs, uterine sound, PVP solution, drape, 2oz cup, half-tray, CSR wrap, sterilization pouch FDA UDI
Model / Reference
BR980-9625 FDA UDI
Description
Disposable IUD Sterile Kit, (5) per box: tenaculum forcep, stitch scissor, swabs, uterine sound, PVP solution, drape, 2oz cup, half-tray, CSR wrap, sterilization pouch FDA UDI

Identifiers

Catalog Number
BR980-9625 FDA UDI
Primary DI / UDI-DI
00840183515270 FDA UDI
FDA Product Code
PXV FDA UDI
GMDN Term
Obstetrical/gynaecological surgical procedure kit, non-medicated, single-use 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Obstetrical/gynaecological surgical procedure kit, non-medicated, single-use

BR Surgical, LLC by Br Surgical Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Obstetrical/gynaecological surgical procedure kit, non-medicated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Br Surgical Llc

Sources (1)

  • FDA UDI 401843b0-75dd-4d9f-8c32-6cc43022291f 35 fields · synced May 30, 2026