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Key Surgical Suture Booties

FDA UDI

Class I (US FDA UDI)

by Key Surgical, LLC

Identity

Trade Name
Key Surgical Suture Booties FDA UDI
Generic Name
Vascular booties FDA UDI
Device Name
Suture Booties, Yellow, Sterile, 5 pair/pad; 5 pads/box FDA UDI
Model / Reference
VB-1115 FDA UDI
Description
Suture Booties, Yellow, Sterile, 5 pair/pad; 5 pads/box FDA UDI

Identifiers

Primary DI / UDI-DI
00849771019138 FDA UDI
FDA Product Code
GDJ FDA UDI
GMDN Term
Vascular booties 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

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Lumen/Inner Diameter — .062 Inch FDA UDI

Category: Vascular booties

Key Surgical Suture Booties by Key Surgical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular booties.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Key Surgical, LLC

Sources (1)

  • FDA UDI 23e8abc1-b929-49eb-ae73-3a1999bca27a 35 fields · synced May 30, 2026