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Retractor, Manual, acc. Parker-Langenbec Fig.1=27x15+40x15mm, Fig.2=31x15+45x15

FDA UDI

Class I (US FDA UDI)

by Geister Medizin Technik GmbH

Identity

Trade Name
Retractor, Manual, acc. Parker-Langenbec Fig.1=27x15+40x15mm, Fig.2=31x15+45x15 FDA UDI
Generic Name
Hand-held surgical retractor, reusable FDA UDI
Device Name
Retractor, Manual, acc. Parker-Langenbec Fig.1=27x15+40x15mm, Fig.2=31x15+45x15 FDA UDI
Model / Reference
30-0490 FDA UDI
Description
Retractor, Manual, acc. Parker-Langenbec Fig.1=27x15+40x15mm, Fig.2=31x15+45x15 FDA UDI

Identifiers

Catalog Number
30-0490 FDA UDI
Primary DI / UDI-DI
04057034108314 FDA UDI
FDA Product Code
GAD FDA UDI
GMDN Term
Hand-held surgical retractor, reusable 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

Category: Hand-held surgical retractor, reusable

Retractor, Manual, acc. Parker-Langenbec Fig.1=27x15+40x15mm, Fig.2=31x15+45x15 by Geister Medizin Technik GmbH — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Hand-held surgical retractor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2b31236a-08fb-47e3-9673-c25e3ebb19c5 35 fields · synced May 31, 2026