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Aesculap

FDA UDI

Class I (US FDA UDI)

by Aesculap, Inc.

Identity

Trade Name
AESCULAP FDA UDI
Generic Name
Skin graft carrier FDA UDI
Device Name
CARRIER PLATE F/BA720R FACTOR 3 FDA UDI
Model / Reference
BA722 FDA UDI
Description
CARRIER PLATE F/BA720R FACTOR 3 FDA UDI

Identifiers

Catalog Number
BA722 FDA UDI
Primary DI / UDI-DI
04038653085170 FDA UDI
FDA Product Code
FZW FDA UDI
GMDN Term
Skin graft carrier 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

No

FDA UDI

Category: Skin graft carrier

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

Similar devices

Also classified as Skin graft carrier.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesculap, Inc.

Sources (1)

  • FDA UDI 4f4de8c6-655d-4c68-86f4-fed61f52c337 35 fields · synced Jun 8, 2026