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Tiger Guard

FDA UDI

Class I (US FDA UDI)

by KimsMed Co., Ltd.

Identity

Trade Name
Tiger Guard FDA UDI
Generic Name
Breast implant delivery funnel, manual FDA UDI
Model / Reference
REF_02KR FDA UDI

Identifiers

Primary DI / UDI-DI
08800071700111 FDA UDI
FDA Product Code
KDD FDA UDI
GMDN Term
Breast implant delivery funnel, manual 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

Yes

FDA UDI

Category: Breast implant delivery funnel, manual

Tiger Guard by KimsMed Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Breast implant delivery funnel, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
KimsMed Co., Ltd.

Sources (1)

  • FDA UDI f02b173b-3ae2-487b-a20d-7e15f4cb141c 33 fields · synced Jun 1, 2026