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Elbow Connector

FDA UDI

Class I (US FDA UDI)

by Obp Corporation

Identity

Trade Name
ELBOW CONNECTOR FDA UDI
Generic Name
Hand-held surgical retractor, single-use FDA UDI
Device Name
SMOKE EVACUATION TUBING CONNECTOR FDA UDI
Model / Reference
C100202 FDA UDI
Description
SMOKE EVACUATION TUBING CONNECTOR FDA UDI

Identifiers

Primary DI / UDI-DI
M648C1002020 FDA UDI
FDA Product Code
GAD FDA UDI
GMDN Term
Hand-held surgical retractor, 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

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: Hand-held surgical retractor, single-use

Elbow Connector by Obp Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand-held surgical retractor, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Obp Corporation

Sources (1)

  • FDA UDI fc42f740-f4b0-4c4c-81df-8599a9b10086 33 fields · synced May 30, 2026