← Back to catalogue

Lid

FDA UDI

Class I (US FDA UDI)

by KLS-Martin L.P.

Identity

Trade Name
LID FDA UDI
Generic Name
Surgical instrument/implant rack FDA UDI
Device Name
FOR MESH TRAY, NON STICK RED BIPOLAR FORCEPS FDA UDI
Model / Reference
55-805-28-01 FDA UDI
Description
FOR MESH TRAY, NON STICK RED BIPOLAR FORCEPS FDA UDI

Identifiers

Primary DI / UDI-DI
00888118125743 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Surgical instrument/implant rack 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

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: Surgical instrument/implant rack

Lid by KLS-Martin L.P. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument/implant rack.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
KLS-Martin L.P.

Sources (1)

  • FDA UDI 5a2aa461-e93d-4e7a-861a-f4f493e8cf45 35 fields · synced May 30, 2026