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Pinnacle

FDA UDI

Class II (US FDA UDI)

by Kerr Corporation

Identity

Trade Name
Pinnacle FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
Clear Patient Chair Sleeve 48x56 (length x width). FDA UDI
Model / Reference
NSC100C FDA UDI
Description
Clear Patient Chair Sleeve 48x56 (length x width). FDA UDI

Identifiers

Primary DI / UDI-DI
00195062147159 FDA UDI
FDA Product Code
PUI FDA UDI
GMDN Term
Medical equipment/instrument drape, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 48 Inch FDA UDI

Category: Medical equipment/instrument drape, single-use

Pinnacle by Kerr Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical equipment/instrument drape, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kerr Corporation

Sources (1)

  • FDA UDI 19db9940-2d1e-48c9-a340-18fa25ec3a54 35 fields · synced Jun 8, 2026