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Medline Renewal

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE RENEWAL FDA UDI
Generic Name
Rigid endoscopic scissors, single-use FDA UDI
Device Name
3622 SUPER-ATRAUMATIC GRABBER CONTROL T FDA UDI
Model / Reference
3622R FDA UDI
Description
3622 SUPER-ATRAUMATIC GRABBER CONTROL T FDA UDI

Identifiers

Catalog Number
3622R FDA UDI
Primary DI / UDI-DI
10888277368330 FDA UDI
FDA Product Code
LRW FDA UDI
GMDN Term
Rigid endoscopic scissors, 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Rigid endoscopic scissors, single-useRigid endoscopic tissue manipulation forceps, reprocessed

Medline Renewal by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic tissue manipulation forceps, reprocessed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI 478f7239-042c-4e56-882a-1c4493382473 35 fields · synced May 30, 2026