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Active Extra Thick Lace Bite Protector

FDA UDI

Class I (US FDA UDI)

by SILIPOS Holding LLC

Identity

Trade Name
Active Extra Thick Lace Bite Protector FDA UDI
Generic Name
Elbow/ankle friction/impact protector FDA UDI
Model / Reference
7224 FDA UDI

Identifiers

Primary DI / UDI-DI
00614464072246 FDA UDI
FDA Product Code
FMP FDA UDI
GMDN Term
Elbow/ankle friction/impact protector FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6450 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Elbow/ankle friction/impact protector

Active Extra Thick Lace Bite Protector by SILIPOS Holding LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Elbow/ankle friction/impact protector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
SILIPOS Holding LLC

Sources (1)

  • FDA UDI 86627c18-b575-471e-ad2a-64d26887826c 32 fields · synced May 30, 2026